The microscopic structure of water Water is a very polar molecule due to the significant electronegativity difference between its elements. Its shape allows for two exposed lone pairs of electrons on the oxygen atom, enhancing its polarity. Water molecules undergo hydrogen bonding. A hydrogen bond is a special type of dipole-dipole attraction between molecules. It arises from the attractive force between a hydrogen atom covalently bonded to a highly electronegative atom such as N, O, or F. A hydrogen bond forms between the negative oxygen side of one molecule and the positive hydrogen side of another molecule. The effect of hydrogen bonding on the unique physical properties of water Water is used all the time, every day, but many of us are unaware of the unusual and unique properties of water, including: ➔ Boiling point and freezing point ➔ Surface tension and vapour pressure ➔ Viscosity and cohesion ➔ Specific heat capacity Boiling and melting point Look at the trends in the boiling points of some hydrides formed with elements in Group 16(VI). The hydride for tellurium: H2Te (hydrogen telluride) has a boiling point of -4 °C. Moving up the periodic table, the next hydride is H2Se (hydrogen selenide) with a boiling point of -42 °C. Further up is H2S (hydrogen sulfide) with a boiling point of -62 °C. The hydride of oxygen, H2O (water), surprisingly has a much higher boiling point of 100 °C. Key terms Melting point - The temperature at which the solid and liquid phases of a substance are at equilibrium. Boiling point - The temperature at which the vapour pressure of a substance equals atmospheric pressure. Heat of vaporisation is the energy that is needed to change a given quantity of a substance into a gas. Surface tension and vapour pressure Besides mercury, the only metal that's liquid at room temperature, water has the highest surface tension among liquids. This is due to hydrogen bonding in water molecules. Water also has a high heat of vaporization. Vaporization occurs when a liquid becomes a gas, classifying it as an endothermic reaction. Vapour pressure is inversely related to intermolecular forces; stronger intermolecular forces result in lower vapour pressure. Water has strong intermolecular forces and a low vapour pressure, meaning it's not easy for water to become a gas. Viscosity Viscosity is the property of a fluid that resists flow. While we often think of honey or motor oil as viscous, water also has noticeable viscosity. Liquids with strong intermolecular forces are typically more viscous than those with weaker interactions. Solid State (ICE) Substances, including water, become less dense when heated and denser when cooled. Thus, cooling water makes it dense, forming ice. Water is special because its solid state floats on its liquid state! Why? This is due to water's unique shape. As water freezes, molecules slow down, forming hydrogen bonds and a structured arrangement. Water’s bent shape means its solid form has spaces between molecules, increasing volume by about 9%. This structure makes ice less dense than liquid water, where molecules are packed closer. For example, a can of coke can explode in a freezer as the water in the coke expands when frozen. Substances, including water, become less dense when heated and denser when cooled. Thus, cooling water makes it dense, forming ice. Water is special because its solid state floats on its liquid state! Why? This is due to water's unique shape. As water freezes, molecules slow down, forming hydrogen bonds and a structured arrangement. Water’s bent shape means its solid form has spaces between molecules, increasing volume by about 9%. This structure makes ice less dense than liquid water, where molecules are packed closer. For example, a can of coke can explode in a freezer as the water in the coke expands when frozen. Water as the "universal solvent" Water is a very polar molecule (dipole) that can dissolve or dissociate many particles. Oxygen carries a slightly negative charge, while the two hydrogens carry a slightly positive charge. Negative particles of another compound are attracted to water's hydrogen atoms, and positive particles are attracted to water's oxygen molecule, causing dissociation. This ability allows many ionic compounds and polar covalent substances to dissolve in water, making it essential for making coffee, most cold drinks, and preparing medicines. Recap of water's important properties Here is a list of the important properties of water dealt with in the last lesson. ➔ Water is the only substance on Earth that naturally exists as solid, liquid, and gas. These changes require heat exchange, crucial for spreading thermal energy in the atmosphere. ➔ Water's high specific heat allows it to absorb much heat before warming and releases it slowly as it cools. This moderates Earth's climate and aids temperature regulation in organisms. ➔ Water conducts heat effectively, second only to mercury, resulting in a large body of water having a uniform temperature. ➔ As a universal solvent, water dissolves many compounds, allowing it to carry nutrients for organisms. Water's high surface tension helps form droplets, allowing water and nutrients to move through plants and small blood vessels in animals. Specific heat capacity The sun is responsible for warming up the Earth through the process of radiation, but if it wasn’t for water the effect on the sun's radiation would be more dramatic. Key term Specific heat capacity is defined by the amount of heat needed to raise the temperature of 1 gram of a substance 1 degree Celsius (°C). Water has a high specific heat capacity, meaning it takes more energy to increase its temperature than many other substances. If we heat a pot of water, which heats first: the pot or the water? The pot heats up faster! Despite applying the same amount of heat, the pot responds quicker. This is because water requires more energy to change temperature. Water exists in three phases on Earth: liquid, solid, and gas. A significant amount of energy is needed to transition between these phases due to water’s high heat capacity. If we leave a bucket of water in the summer sun, it will warm up, but not boil an egg. Walking barefoot on black tar roads in South African summers would burn our feet. Dropping an egg on a car hood on a very hot day might fry it. Metals have a much lower specific heat than water. Water allows organisms to endure various weather conditions. Ice expands as it freezes, which is why it floats on water. In winter, when a lake starts to freeze, the surface forms ice and moves deeper, allowing skating and support on frozen lakes. If ice sank, lakes would freeze bottom-up, killing ecosystems. Because ice floats, fish survive under it in winter. The ice surface insulates the lake from cold air, maintaining water temperature suitable for lake ecosystems. https://youtu.be/v9hm1Ym9E-8 Electromagnetic radiation Light is electromagnetic radiation detectable by our eyes, carried by electromagnetic waves. These waves travel at light speed (symbol c), which is 3 x 108 m.s-1 (300 000 000 m.s-1) in a vacuum. Einstein stated nothing exceeds this speed. The visible spectrum has wavelengths from 400–700 nanometers. Other electromagnetic radiation includes microwaves, X-rays, radio waves, and ultraviolet light. These varieties differ in wavelengths and frequencies. Electromagnetic waves occur when a charged particle accelerates, creating an electric field that produces a perpendicular magnetic field, and vice versa. The interaction of these fields propagates the wave. The electromagnetic spectrum The electromagnetic spectrum includes a range of waves with different frequencies and wavelengths, encompassing both visible and large invisible components. Frequency and wavelength share a special relationship. A proportionality compares two quantities. An inversely proportional relationship means as one increases, the other decreases proportionally. As frequency increases, wavelength decreases at a constant speed of 3x 108m.s-1. Thus, frequency and wavelength are inversely proportional. fαλ where: f is the frequency λ is the wavelength. These waves will range from extremely low frequencies to extremely high frequencies. The following is the range of electromagnetic waves in order of increasing frequency (or decreasing wavelength). ➔ Radio waves (lowest frequency / highest wavelength) ➔ Microwaves ➔ Infra-red ➔ Visible light ➔ Ultraviolet ➔ X-rays ➔ Gamma rays (highest frequency / lowest wavelength) Figure 1: The electromagnetic Spectrum in order of increasing frequency Light has all the properties of waves: ➔ Light travels in straight lines ➔ Light is reflected ➔ Light is refracted ➔ Light is diffracted Where does light come from? Light comes from a luminous source like the sun, a light bulb, or a candle. We also perceive light when it reflects off surfaces, making them illuminated sources, e.g., the moon, a mirror, or any visible object. Light is an electromagnetic wave with dual characteristics: wave and particle nature. Why is light important? Light is a form of energy (radiant energy) that plants use to make food in the process of photosynthesis. No life could exist on Earth without this process. Light rays In geometrical optics, which models light travel, light is described by rays. This accurately represents wave behavior. Geometric optics covers reflection, refraction, and diffraction. What happens when light strikes an object? All objects are transparent, translucent, or opaque. Transparent objects let light pass through with minimal resistance, allowing clear visibility. Translucent objects let some light through but diffuse or scatter it. Visibility is unclear. Examples: Some plastics, coloured glass, cotton cloth. Opaque objects absorb or reflect light, blocking it entirely. Visibility is impossible. Examples: Mirrors, wood, metal. Key term A light ray is a hypothetical model of light, where light is drawn as a straight line with arrows to represent direction. A ray diagram is simply a diagram that shows the path of light rays Figure 1: Ray diagram of light from the bulb to eye. Key terms Incident ray - the ray of light coming towards the surface. Reflected ray - the ray of light moving away from the surface Normal - The line, which is perpendicular to the plane of the surface. Angle of incidence (θi) - The angle between the normal to a surface and the incident light ray Angle of reflection (θr) - The angle between the normal to a surface and the refracted light ray. Figure 2: Light reflecting off a mirror. There are two rules associated with reflection The angle of incidence is equal to the angle of reflection The normal, the angle of incidence and angle of reflection all lie on the same plane (nothing goes through the surface Applications of reflection in daily life A parabolic reflector A parabolic reflector is a mirror or dish with a parabolic shape (similar to the parabola in mathematics). Parabolic reflectors are used in car headlamps, torches, and telescopes. Figure 5: Parabolic mirror of a headlamp. Fun fact South Africa is a world leader in astronomy and we have some remarkable telescopes. Gigantic galaxies have been discovered with the MeerKAT telescope which is found near the small Northern Cape town of Carnarvon. The SKA (Square Kilometer Array) project aims to create the world’s largest radio telescope, with a square kilometre of collecting area. It will be situated in Africa and Australia. The SKA will offer an unmatched scope in observations, surpassing the Hubble Space Telescope's image resolution by 50 times and can image vast sky areas. Binoculars and Microscopes These are apparatuses you might have seen before. Binoculars magnify distant objects, using glass prisms that act as mirrors. Microscopes observe small or invisible objects. They magnify images through at least one lens. Speed of light When Einstein developed the Theory of Relativity, he found that light travels at a constant speed of 299 792 458 m.s-1. We round that number up to 3 x 108 m.s-1. What is a vacuum again? A vacuum in physics is a space with no matter in it. Not even gas molecules. The symbol that we use for the speed of light is lowercase c. On the data sheet that you are given in exams and tests, you will be given this constant as c = 3 x 108 m.s-1. Refraction The refraction of light is a very commonly seen phenomenon. Other waves such as water waves and sound waves can also undergo refraction. Key term Refraction of light is the change in direction of a light ray due to a change in speed when light travels from one medium into the other of a different optical density. Optical density is a measure of the refracting power of a medium. When light moves between optical media, it changes speed based on the medium's density. A denser medium results in slower light speed. This is known as optical density. The higher the optical density, the slower the speed of light in that medium. We'll later list the speed of light in various mediums and learn to calculate it ourselves. Let's understand why light slows in denser mediums. When light travels from a vacuum into air, it slows down. Light protons are absorbed and re-emitted upon encountering a particle, taking time and thus slowing down. In grade 10, we learned about matter phases: gases, liquids, and solids. In gases, particles are far apart; in liquids, they are closer; and in solids, they are extremely close together. Therefore, if light travels from a vacuum into air, it slows down, and if it goes from air to water, it slows down further. What if light enters glass? It would be slower because the particles are closer together. The greater the speed difference of light between two mediums, the more it refracts or bends as it transitions between them. Key term The refractive index of a material is the ratio of the speed of light in vacuum (c) to the speed of light in a material (v). n=c/v Where: n is the refractive index c is the speed of light in a vacuum v is the speed of light in the other medium There are no units for the refractive index as the units for the denominator and numerator would cancel out. Study tip You do not need to learn the speeds of light in various mediums or their respective refractive indices. Below is a list of refractive indices for some transparent substances. You don't need to memorize it, but reviewing the table may help you notice trends between the type or phase of substance and the refractive index. Table 1: Refractive indices of some optical media MATERIAL REFRACTIVE INDEX Vacuum 1 Air 1,0003 Water 1,33 Paraffin 1,44 Glass 1,52 Diamond 2,42 By examining the table, you'll notice that the refractive index increases as substances become denser. Diamond, one of the hardest materials on earth, is very dense with a high refractive index. Remember, a larger refractive index means slower light speed in that medium. Refraction in everyday life A rainbow A rainbow is caused by refraction and reflection of light. Light entering a water droplet is refracted into seven colours. It is then reflected off the droplet's back. As it exits, the light is refracted again at various angles. Figure 3: Refraction of light in a drop of water Twinkling Stars The atmosphere's air varies in thickness. Some areas are denser than others. At night, stars seem to twinkle because light refracts while passing through the atmosphere's different layers. Fish Bowl If you've seen an aquarium or fish bowl, you might notice the fish appear bigger through the side. Even your hand seems larger on the opposite side. This is due to light refraction through the glass and water, making things look slightly lifted and bigger. Try it at home by passing your hand behind a glass of water to see the effect. What are refraction ray diagrams? In the last section, you learned about refraction. Recap: Refraction occurs when light moves between different optical media. It will slow down or speed up, depending on whether it travels from a denser to a less dense medium. To understand this, imagine pushing a shopping trolley onto grass. If aligned straight with the grass, the trolley slows as wheels hit the grass. Similarly, light approaching from air to glass slows down. There's no bending or refraction if light meets the surface perpendicularly, as it is on the normal line. Figure 1: Light travelling from air to glass perpendicular to the surface. What would happen to the trolley as it approached the grass from the pavement at an angle? First, look at the diagram and then read through the explanation Figure 2: Trolley going from pavement to grass. When the right front wheel goes into dense grass it slows down, but the left front wheel continues at the same speed. This causes the trolley to turn slightly to the right, towards the normal, which is perpendicular to the surfaces. This analogy helps illustrate what happens when light travels through different mediums and how it can be refracted. Key terms Angle of incidence: The angle between the normal to a surface and the incident light ray. Angle of refraction: The angle between the normal to a surface and the refracted light ray. Light travelling from less dense to more dense mediums If light travels from a less dense medium like air into a more dense medium like water, it slows down. This is because water has a higher refractive index than air. The light bends towards the normal, making the angle of incidence greater than the angle of refraction. Figure 3: Light travelling from less dense to more dense medium. As you can see, the angle of refraction is less than the angle of incidence when light travels from a less dense to a more dense medium. θi > θr In the next module, we will learn about how to calculate various variables related to refraction using a principle called Snell’s law. Light travelling from more dense to less dense medium If light transitions from a denser medium like glass to a less dense medium like air, it speeds up due to air having a lower refractive index than glass. The light bends away from the normal, resulting in a refraction angle greater than the incidence angle. Figure 4: Light travelling from a more dense to a less dense medium. As you can see the angle of incidence is less than the angle of refraction when light travels from a more dense to a less dense medium. θi < θr Ray diagrams through various prisms Let's look at some examples of when light passes through different transparent prisms and draw the respective ray diagrams. Key term A prism is a 3D shape which has a constant cross section, i.e. both ends of the solid are the same shape. Some revision In the previous lesson, we learned that light can undergo refraction. Refraction occurs when light transitions from one optical medium to another with different optical densities. The light's speed changes, and its direction often alters. As light passes between different optical media, it slows down or speeds up based on the medium's density. The denser the medium, the slower the light travels. This concept is known as optical density. Key terms Angle of incidence: The angle between the normal to a surface and the incident light ray. Angle of refraction: The angle between the normal to a surface and the refracted light ray. Refractive index ( n ) of a material is the ratio of the speed of light in vacuum (c) to the speed of light in a material (v). n=c/v Where: n is the refractive index c is the speed of light in a vacuum (3 x 108 m.s-1) v is the speed of light in the other medium Light travelling from less dense to more dense mediums When light travels from a less dense medium like air into a denser medium such as water, it slows down because the refractive index of water is higher. The light bends towards the normal, making the angle of incidence greater than the angle of refraction. The angle of refraction is less than the angle of incidence in this scenario. θi>θr Light travelling from denser to a less dense medium When light travels from a denser medium like glass to a less dense medium such as air, it speeds up. This is because the refractive index of air is lower than that of glass. The light bends away from the normal, making the angle of refraction greater than the angle of incidence. The angle of incidence is less than the angle of refraction when light moves from a denser to a less dense medium. θr>θi Snell's law This law was discovered in 1621 by the Dutch astronomer and mathematician Willebrord Snell (also called Snellius). Snell's law remained unpublished until mentioned by Christiaan Huygens in his treatise on light. Watch the short video to learn more about his impact on physics and astronomy. Key term Snell's Law: The ratio of the sine of the angle of incidence in one medium to the sine of the angle of refraction in the other medium is constant. If you look at the table, do you notice a trend? As the material becomes denser (diamond is denser than air), the refractive index increases. The formula for Snell's law is: ni × Sin Θi = nr × Sin Θr Where: ni is the refractive index of incident ray nr is the refractive index of refracted ray θi is angle of incidence θr is angle of refraction Snell's formula is: ni⋅sinΘi=nr⋅sinΘr The gradient of this graph is: m=ΔyΔx If you manipulate Snell's formula, you get: m=sinΘrsinΘi sinΘrsinΘi=ninr So you can see finding the gradient can be useful. In the last module, we learned how to use Snell’s law to calculate a missing variable when light is refracted from one optical medium into another using this formula. ni×Sinθi=nr×Sinθr Key term Snell's Law: The ratio of the sine of the angle of incidence in one medium to the sine of the angle of refraction in the other medium is constant. Figure 2: Effect of changing the angle of incidence on the angle of refraction. As you can see the angle of refraction is less than the angle of incidence when light travels from a less dense to a more dense medium. θi>θr So even if the angle of incidence increases to 90°, the angle of refraction would be less than 90°. Now let’s consider a situation where light is travelling from a denser to a less dense medium. We know that the light will bend away from the normal thereby making the angle of refraction greater than the angle of incidence. Figure 3: Effect of changing the angle of incidence on the angle of refraction. Figure 4: Increasing the angle of incidence. You will notice that as the angle of incidence increased, so did the angle of refraction. If the angle of incidence increased to the point that the angle of refraction became 90°, then that angle of incidence is called the critical angle. Figure 5: Increasing the angle of incidence until it reaches the critical angle. When this happens the refractive ray lies on the boundary between the two mediums and no light goes into the second medium. Key term Critical angle is the angle of incidence in the optically denser medium for which the angle of refraction in the optically less dense medium is 90°. Study tip When calculating the critical angle, light is always travelling from a denser to a less dense medium and the angle of refraction is 90°. If the angle of incidence exceeds the critical angle for the medium, a phenomenon called total internal reflection takes place. For any angle of incidence larger than the critical angle, you can’t use Snell's law to solve for the angle of refraction, because it will show that the refracted angle has a sine larger than 1, which is not possible. Figure 2: Increasing the angle of incidence until it reaches the critical angle. In that case, all the light is totally reflected off the boundary, obeying the laws of reflection. So the light does not go through the surface but rather is reflected off the surface. Figure 3: Increasing the angle of incidence until it reaches the critical angle Conditions for total internal reflection: ➔ The light ray moves from a more dense medium to a less dense medium. ➔ The angle of incidence must be greater than the critical angle. Application of Total Internal Reflection Optical fibers Optical fibers are based entirely on this principle of total internal reflection. An optical fiber is a flexible strand of glass. A fiber optic cable is usually made up of many of these strands, each carrying a signal made up of pulses of laser light. The light travels along the optical fiber, reflecting off the walls of the fiber. With a straight or smoothly bending fiber, the light will hit the wall at an angle higher than the critical angle and will all be reflected back into the fiber. Even though the light undergoes a large number of reflections when travelling along a fiber, no light is lost. Figure 4: How fiber optics work in a glass tube. Fiber Optics in Surgery and Dentistry Fiber optic cables are widely used in the fields of medicine. An important part of non-intrusive surgical methods is known as an endoscopy. A non-invasive procedure is a treatment that does not require large incisions (cutting) into the body or the removal of tissue. In these applications, a fiber optic light is used to light up the surgery area within the body, making it possible to reduce the number and size of incisions made. Fiber optics are also used in microscopy and biomedical research. Fiber optics in telecommunications Fiber optic cables have transformed telecommunications and connectivity. Fiber technology is a game changer. Through fiber cables, signals can be sent across the world at the speed of light. They are quite often laid on the seabed between countries. Fun fact The South Africa Far East cable is an optical fiber submarine communications cable linking Melkbosstrand and Mtunzini, South Africa to Penang, Malaysia. It has a total length of 13,104 kilometers and is one of a pair of cables that provides high-speed digital links between Europe, West and Southern Africa, and the Far East. These are only some of the common uses. There are many more applications of fiber optics. Spend some time after the lesson researching what other interesting applications of fiber optics there are. Huygens's principle What is Huygens's principle? In 1670, Christiaan Huygens was the first to describe how wave theory may also account for the principles of geometric optics. Of course, no one was paying attention to him at that moment. Only later after wave theory was accepted, was his work rediscovered. Huygens had a crucial insight into the physics of wave propagation that is now known as the Huygens principle. Key term Huygens's principle states that every point of a wave front serves as a point source of spherical, secondary waves that move forward with the same speed as the wave. To understand Huygens's principle, we will break down the definition into smaller components. Every point of a wavefront serves as a point source - on the last page we saw that if you look at the top of a wave, it is made out of a series of points. These points all are a source of small circular secondary wavelets, which is simply a term for small waves. Figure 11: Wavelets produced on a wavefront The new wavefront is drawn by drawing a tangent of all the new wavelets Figure 12: Wavelets produced a new wavefront using a tangent. Limitations of Huygens's principle Although it is still used today there are some drawbacks and limitations to Huygens's principle. The principles of Huygens generally failed to explain the photoelectric effect which you will find about in Grade 12. A serious drawback is that the theory proposes an all-pervading medium required to propagate light known as the ether which is a theoretical universal substance believed during the 19th century to act as the medium for transmission of electromagnetic waves. The ether was later proven not to exist. Study tip A typical exam question that you could get on Huygens' principle is to state TWO changes that could be made to change the appearance of a diffraction pattern if green monochromatic light is used. Wavefronts We have looked at two properties already that show the wave nature of light reflection and refraction. In this and the next lesson we will look at diffraction. A quick reminder: Reflection is the bouncing off of light off a surface. Refraction is the bending of light as it slows down or speeds up as it moves from one optical medium to another. Key term ❖ A transverse wave is a wave in which the particles of the medium vibrate at right angles to the direction of motion of the wave. A transverse wave is a succession of transverse pulses. ❖ Diffraction is the ability of a wave to spread out in wavefronts as the wave passes through a small aperture or around a sharp edge. Waves are not stationary so when you look at the image below remember that the wave is moving. Figure 2: Transverse wave What you can understand is that the crest or trough is not a single particle but rather a collection of many particles or points all on the crest or on the trough. We will represent these particles next to each other on the crest with dots in the diagram below. The dots (red for crest) are all the particles that have reached their maximum displacement from the rest position. The dots (orange for trough) are all the particles that have reached their maximum displacement. All the red points on one crest and all the orange points on one trough are all in their maximum position from the rest position. So these adjacent points are in phase and next to each other. This is a specific term called wavefront. Figure 5: Transverse wave from above. Key term A wavefront: An imaginary line joining points on a wave that are in phase. Make sure that you don’t get confused between wavelength and wavefront. A wavelength is the distance between two successive points in phase Superposition When two or more pulses occur at the same time in the same location, they will superimpose on each other. This means that their amplitudes will combine at the points where they occur at the same time. Pulses can either interfere constructively or destructively depending on whether the resulting amplitude is greater than or less than the amplitudes of the original pulses. After the pulses superimpose on each other they continue in their original direction and assume their original amplitude. Key term The principle of superposition states that when two pulses occur in the same place at the same time, the resulting pulse is the sum of the two interfering pulses. Pulses can have their amplitudes in different directions from each other. For this lesson we will say that a pulse that goes up will have a positive amplitude and pulses that go down have a negative amplitude. Constructive interference When two pulses constructively interfere, their resulting amplitude is greater in magnitude than each of the original pulses. This happens when both pulses have their amplitudes in the same direction. Key term Constructive interference occurs when the resulting amplitude of two or more pulses during interference is greater than the amplitude of the original pulses. Figure 6: Constructive interference is shown in this diagram. Interference When two pulses destructively interfere their resulting amplitude is smaller than the amplitudes of the original pulses. This happens when two pulses have amplitudes in opposite directions. Key term Destructive interference occurs when the resulting amplitude of two or more pulses during interference is less than the amplitude of the original pulses. Figure 8: Destructive interference is shown in this diagram. Diffraction around a corner Have you noticed that sound seems like it can bend around a corner? You could be standing on the other side of the door and still hear people on the other side of the door. The bending of the sound wave is because the wave is diffracted. If you examine the wave diagram above, you will see that the red points on wavefront A, produce wavelets. Those wavelets, in turn, produce wavefront B. When wavefront B collides with the barrier, only some of the wave moves forward. If you look carefully at wavefront C, the part of the wave closest to the barrier starts to curve due to the wavelets. Wavefront C now produces more wavelets but because it is curved, the curved end will still produce wavelets but they will not be moving forward but at an angle upwards to form wavefront D. Diffraction through a gap When a water wave or a light wave goes through a gap, how will it bend? We can use Huygens' principle once again to predict the shape of the wave as it goes through a gap. . Figure 15: Sound diffraction through a doorway When a water wave or a light wave goes through a gap as shown below, how will it bend or diffract? You guessed it! We can use Huygens's principle once again to predict the shape of the wave as it goes through a gap. Figure 16: Wavefront going through a gap If you examine the wave diagram above, you will see that the red points on wavefront A, produce wavelets. These wavelets, in turn, produce wavefront B. When wavefront B collides with the barrier, only some of the wave moves forward. If you look carefully at wavefront C, the part of the wave closest to the barriers on both sides starts to curve due to the wavelets. Wavefront C now produces more wavelets but because it is curved, the curved end will still produce wavelets but they will not be moving forward but at an angle outwards to form wavefront D. When waves collide with barriers, they can undergo diffraction. What causes this to happen? It becomes evident when we apply Huygens' principle. Consider a wavefront approaching a barrier with a slit in it: only the points on the wavefront that move into the slit can continue emitting forward-moving waves. However, because a large portion of the wavefront is blocked by the barrier, the points on the hole's edges emit waves that bend around the edges. As the wavefront (see Figure 1) approaches the gap it produces wavelets as Huygens's principle says. Figure 1: Wavefront approaching gap. As the wavefront strikes the barrier, only the portion of wave that can go through the gap will continue. The rest of the wave will be reflected off the barrier. If you look at figure 2, you can see that as the wavefront passes through the opening, it produces wavelets and they in turn produce a new wavefront. This wave is diffracted or bent as shown in the diagram below. Figure 2: Wavefront going through a gap. Diffraction patterns When the light comes through the narrow slit (gap) and if we placed a screen a distance away from the gap. What do you think you would see on the screen? We are going to use Huygens's principle as well as our understanding of constructive and destructive interference and see the diffraction pattern on the screen. Wavefronts are emitted by each point (A and B) source from the slit's edge. A succession of wavefronts emitted from each point source is seen in the diagram. The dashed lines represent troughs in the waves emitted by the point sources, while the black lines represent peaks in the waves emitted by the point sources. With a solid red dot, constructive interference (peak meets peak or trough meets trough) occurs, and with a circle, destructive interference (trough meets a peak) occurs. There will be spots on the barrier where constructive interference occurs and places where destructive interference occurs when the wavefronts reach a barrier. Figure 3: Wavefront going through a gap. Two properties of waves, diffraction and interference, produce a pattern of constructive and destructive interference measured at a distance from a single slit. This pattern is sometimes referred to as an interference pattern and other times as a diffraction pattern. For a single narrow slit, the intensity of the diffraction pattern looks like this: figure 4: Diffraction pattern on a screen. The peak that is the highest (in the middle) shows the greatest intensity. Intensity can be understood by the amount of light. It is where many waves undergo constructive interference and therefore is a bright section on the screen. We will see this more in a section of the module coming up soon. Remember that the red dots show where constructive interference takes place and at that point, the screen will be lighter/brighter. The white dots show where a crest and a trough meet and destructive interference takes place. Those areas will be darker. Note that this also works for sound waves. If two peaks had to meet with a sound wave it would result in a bigger wave but if a crest and trough had to meet then the waves would cancel out . Effect of slit width and wavelength on diffraction patterns Have you ever attempted to push plasticine through a small hole? Maybe not, but if you have, you've probably observed that it bulges when it passes through the hole. When waves pass through small gaps or push past obstructions, the same thing happens. When we consider waves, there are a couple of factors that cause the diffraction to be more or less. We are going to look at them now. Wavelength The amount of diffraction depends on the wavelength, with longer wavelengths being diffracted at a greater angle than shorter ones. The longer the wavelength of the wave the larger the amount of diffraction. Wavelength The amount of diffraction depends on the wavelength, with longer wavelengths being diffracted at a greater angle than shorter ones. The longer the wavelength of the wave the larger the amount of diffraction. Key terms Wavelength: The distance between two successive points in phase. Frequency: The number of wave pulses per second. Figure 5: Effect of wavelength on diffraction. Slit width The amount of diffraction also depends on the size of the aperture, or gap. The narrower the slit, the more diffraction (bending) will take place. Therefore: diffraction∝1w Where: w is the width of the slit. Figure 6: Effect of slit width on diffraction. Both the above waves have the same wavelength but the slit width is smaller on the right. As you can see on the wave on the left, there is a small amount of diffraction but on the wave on the right there is more diffraction (more bending) as it goes through the opening. Which type of wave, a sound or a light wave, will have greater diffraction? It is a sound wave because a light wave has much higher frequencies than sound waves and therefore will experience less diffraction. Light waves have wavelengths between 400 nm to 700 nm, where n is nano which is x10-9 so 400 nm is 0,0000004 m but an average sound wave has a wavelength of 17 m and 17 mm which is the reason sound waves diffract considerably more than light waves. Figure 7: Comparing diffraction of a light and sound wave. Wave nature of light We know from grade 10 that there are range of electromagnetic waves. They range from long wavelengths with low frequencies to very short waves with very very frequencies. The graphic below shows the electromagnetic spectrum. Radio waves have very long wavelengths (x103 m) but low frequencies (104 Hz). As you move towards the right, the wavelength decreases but the frequencies increase as they are inversely proportional to each other. The same applies to visible light in the middle of the spectrum. Red light has the longest wavelength and will diffract the most but violet light with a shorter wavelength will diffract the least. When we shine monochromatic light (light of one frequency and colour) through a single slit and shine it onto a surface, what can we expect to see? Remember, what are the factors that affect diffraction? It is the width of the slit as well as the wavelength of the wave. The greater the slit width, the less the diffraction, and the longer the wavelength, the greater the diffraction. We know that red light has a longer wavelength and will experience more diffraction as it goes through a single slit. Violet light has a higher frequency and shorter wavelength and will have less diffraction. Green light is in between violet and red. Below is the diffraction pattern of red, violet, and green light as it went through a single slit and was projected onto a screen. Look closely at them and see if you can notice something about the pattern. Figure 9: Diffraction pattern of violet, green, and red light. If you look carefully you will observe that the central band for red is wider than green and violet. That is because red light has a lower frequency and longer wavelength which means that it will diffract more than both green and violet light. The dark bands on the screen are areas where destructive interference takes place (where a crest and trough meet) and this causes the waves to be cancelled out causing a dark area. What is Kinetic molecular theory? We already know that all matter is made up of particles. The kinetic molecular theory says that the particles that make up a substance have a certain amount of kinetic energy (movement energy), meaning that they are all moving, and the way in which they move is responsible for the physical state of matter. Study tip Do you remember covering the Kinetic molecular theory in grade 10? How did we make this model? Whenever we devise a scientific theory that we want to apply, we always have to justify that the theory agrees with the observations that we make. Let’s have a look at how scientists verified the Kinetic molecular theory. To do this, we first have to look at diffusion. Diffusion is the movement of particles from a high concentration to a low concentration. Diffusion takes place in both liquids and gases. Have you noticed sometimes that when someone sprays deodorant in one part of the room, in a few minutes you can smell it on your side of the room? What happens is that the gas molecules in the air, which are in constant motion, collide with the gas molecules of the deodorant and push them around until you smell them. Key term Diffusion is the movement of particles from a high concentration to a low concentration. Diffusion takes place in both liquids and gases. In 1828, a scientist named Robert Brown was trying to study pollen under the microscope. To achieve this he put the pollen in some water, hoping that he would get a clearer view if the pollen was suspended on the water. To his surprise, no matter how still he was trying to keep the sample, the pollen kept moving around on top of the water, not allowing him to have a good look. Through this, he accidentally verified the particular nature of matter and this phenomenon became known as Brownian motion. Phases of matter The different phases of matter You know that matter is found in three phases and that most matter can change from one phase to another by the addition or removal of heat energy. Let’s revise the properties of solids, liquids, and gases quickly to ensure that we know how to distinguish between them. Solids In a solid, the particles are packed tightly together and have little kinetic energy. The particles have strong intermolecular forces and they don’t have enough energy to overcome the forces between them, so the particles vibrate in place. This explains why solids have a fixed shape and volume. The particles vibrate (slight motion) but stay in their crystal structure. Liquids In a liquid, the particles have more kinetic energy than in a solid. The particles have enough energy to overcome the forces between them, so they can move around freely amongst one another. The particles tend to move wherever they can reach inside the container which is why the liquid takes the shape of the container. The spaces between the particles are bigger in a liquid than in a solid. This means that the forces between the particles are weaker than in a solid; although it is important to note that there are still forces between the particles, they are just not as strong as they are in a solid. Sometimes particles on the surface of a liquid have enough energy to overcome the intermolecular forces of the particles below and can escape from the liquid phase. Gases In a gas the particles have even more kinetic energy than in a liquid. The particles have more than enough kinetic energy to overcome the forces between them so they move wherever they can reach. This also means that the spaces between the particles are much bigger than in a liquid, making the forces between the particles smaller. In a closed container, the particles of a gas will have so much energy that they collide with the walls of the container. This is why a balloon will expand when you add more air, because the air particles collide with the sides of the balloon pushing outwards and expanding the balloon. The kinetic theory of gases can be stated as follows: Gases are made up of particles (e.g. atoms or molecules). The spaces between the particles are large in comparison to the size of the particles. These particles are in constant motion due to their kinetic energy (movement energy). All the particles move in straight lines but at different speeds. The force of attraction between particles is weakest between gas particles. The collisions between particles and the walls of the container do not change the kinetic energy of the system. Ideal gas properties Gases can be somewhat difficult to understand. They are made up of billions upon billions of energetic molecules that might collide and interact. Precisely because it's difficult to describe a real gas, the concept of an ideal gas was created. It was developed as a rough estimation that may be used to simulate and predict the behaviour of real gases. Key term An ideal gas has identical particles of zero volume, with no intermolecular forces between them. The atoms or molecules in an ideal gas move at the same speed. The term "ideal gas" describes a hypothetical gas made up of molecules that obey these rules: The particles are identical in all ways. Their molecules occupy no volume. They have no intermolecular forces between the molecules. The collisions between the particles and the walls of the container are perfectly elastic (which means that they do not lose energy). Ideal gases do not exist in the real world! Real gases behave more or less like ideal gases except at high pressures and low temperatures. The real gases that behave the closest to ideal gases are H2 and He. We will learn more about how we use ideal gases in the next lesson on Boyle’s law but for now, let’s discuss how real gases can deviate from the behavior of ideal gases. Terms used in gases First, let's look at some terms that you will need to know for this entire module and the next. Pres sure Pressure is the force applied over an area. So if you push your flat hand on the desk, you are applying a force on that area. If you now push with just your finger, the pressure will increase because you are pushing with the same force but the area of your finger is smaller than the area of your hand. Figure 1: Pressure exerted by hand compared to finger. In gases, it is slightly different. The pressure is caused by the collisions of the gas particles on the side of the container. More collisions of the particles will result in a higher pressure. The unit for pressure is Pa which is named after the scientist Blaise Pascal. 1 pascal is a pressure of one newton per square metre or N.m-2 Figure 2: 1 Pascal of pressure. For you to get a feel for 1 pascal of pressure, it is roughly the same as the pressure exerted by one piece of ordinary A4 paper placed on a table. It is not a big force per unit area and that is why we very often measure pressure in kPa or MPa or even GPa. You might have heard the term atmospheric pressure before, but what is it? The air surrounding you is made of molecules, and although each molecule is very, very light, the combined effect is that billions and billions of molecules push against everything they come into contact with. Atmospheric pressure, or air pressure, is the name given to this pressure. The air above a surface exerts a force on it as gravity pulls it to Earth. We measure atmospheric pressure at sea level because the level of the sea around the world is constant. The higher you are above sea level, the lower the atmospheric pressure. An atmosphere corresponds to the pressure applied by a vertical column of mercury (like a barometer) with a height of 760 mm. Standard atmospheric pressure, also known as an atmosphere, corresponds to a force of 101,325 pascals (Pa) or Newtons per square meter. Study tip 101 300 Pa = 1 atm and 101 300 Pa = 760 mm Hg (Hg is the symbol for mercury) Please take note that in the three gas laws that follow, the unit for pressure can be given in any of these forms as long as both sides of the equation have the same unit. Fun fact Why do your ears pop? Sudden changes in air pressure, such as when flying, scuba diving, or climbing a mountain, can cause the eardrum to swell and feel blocked. Your ears pop out to regain the same pressure on the inside of the ear and the outside of the ear. Temperature It is easy, even in Physical science, to get terms such as heat and temperature mixed up. Heat and temperature are not the same things. Heat is a form of energy, and describes the transfer of thermal energy between molecules. Its unit is Joules. Temperature is how hot or cold something is or even better, describes the average kinetic energy of molecules in a system. It is measured in Celsius (°C), Kelvin(K), or Fahrenheit (°F) as is used in the United States of America. UCT-KeyTerm Key term The temperature of a substance is a measure of the average kinetic energy of the particles. The faster the particles move, the more kinetic energy they have and therefore the higher the temperature. Although we can get very hot temperatures, such as the surface of the sun at 5800 °C, or as hot as a supernova. A supernova is a transitory event that marks the end of a star's life. The star's existence comes to a dramatic end with one of the greatest explosions ever seen in space. During the explosion, temperatures at the core reach 100 billion degrees Celsius. Although temperatures can vary widely, as you saw above, the coldest temperature we can go to is -273 °C which is called absolute zero. At this point all substances are solid and the particles stop vibrating. In this and the next module, we will be using the Kelvin temperature scale so you will need to know how to convert from degree Celsius to kelvin and back again. The symbol for temperature is t but for absolute temperature it is T. 0 K = -273 °C To convert from degrees Celsius to kelvin: T=t+273 To convert from kelvin to degrees Celsius: t=T−273 STP in chemistry is the abbreviation for Standard Temperature and Pressure. STP is most commonly used when performing calculations on gases. The standard temperature is 273 K (0° Celsius) and the standard pressure is 101 kPa which is atmospheric pressure at sea level. At STP, one mole of gas occupies 22,4 dm3. Key term Volume is how much space an object or substance takes up. There are 100 cm in 1 m so there are 100 cm x 100 cm in 1 m2 There are 100 cm x 100 cm x 100 cm in 1 m3. To convert from m3 to cm3, you must multiply by 1 000 000 or x 106. There are 10 dm in 1 m so there are 10 dm x 10 dm in 1 m2 There are 10 dm x 10 dm x 10 dm in 1 m3. To convert from m3 to dm3, you must multiply by 1 000 or x 103. 1000 L = 1 m3 There are 10 cm in 1 dm, so there are 10 cm x 10 cm in 1 dm2 There are 10 cm x 10 cm x 10 cm in 1 dm3. To convert from dm3 to cm3, you must multiply by 1 000 or x 103. Deviation of a real gas from an ideal gas The term deviation simply means to depart from. It means that at some point real gases stop behaving like ideal gases. In most cases real gases obey the ideal gas rules but when do they stop? Let’s find out what happens when real gases reach high pressure and very low temperatures. When we spoke about an ideal gas, we said that an ideal gas has identical particles with zero volume and there are no intermolecular forces between the particles in the gas. When the pressures are really high and the molecules are compressed, the volume will decrease. The volume will approach a very small number but will not be zero because the molecules will occupy some space that cannot be compressed further. As a result, the pressure of a real gas is higher than it would be for an ideal gas. You can see this when you try to compress a syringe but block the end with your finger. You feel the pressure on your finger, but push as hard as you want, the syringe will not be totally compressed. Figure 12: Gases deviate from ideal gas behaviour at high pressure. The intermolecular forces become greater at low temperatures because the molecules slow down and the molecules are closer together. As the attractive force between molecules grows, the molecules slow down, and there are fewer collisions. As a result, the gas's pressure at low temperatures is lower than what would be predicted for an ideal gas. A real gas will liquefy if the temperature is low enough or the pressure is high enough Figure 13: Gases deviate from ideal gas behaviour at low temperatures. Study tip Real gases deviate from the behaviour of ideal gases under very high pressures and very low temperatures. Quick summary The kinetic molecular theory says that the particles that make up a substance have a certain amount of kinetic energy (movement energy), meaning that they are all moving, and how they move is responsible for the physical state of matter. Matter is found in three phases - solids, liquids, and gases. The distance of the particles in a gas is greater than in a liquid and solid. The particles in a liquid also have more kinetic energy as they move faster. UCT-KeyTerm Key term An ideal gas has identical particles of zero volume, with no intermolecular forces between them. The atoms or molecules in an ideal gas move at the same speed. The term "ideal gas" describes a hypothetical gas made up of molecules that obeys these rules: The particles are identical in all ways Their molecules occupy no volume They have no intermolecular forces between the molecules The collisions between the particles and the walls of the container are perfectly elastic (which means that they do not lose energy) There are four factors that are considered in gas laws. Pressure, volume, temperature and amount of gas. Pressure exerted by a gas is the collisions of the molecules with the walls of the container. The temperature of a substance is a measure of the average kinetic energy of the particles. Volume is how much space an object or substance takes up Real gases deviate from the behaviour of ideal at very high pressures and very low temperatures. What is Boyle’s law? If you take an inflated balloon and squash it, you know that at some point the balloon will burst. It is easy to simply say the squashing burst the balloon, but what is taking place inside the balloon causing it to burst really has to do with the relationship between pressure and volume of the balloon. Look at the video below of a balloon bursting in slow motion when it is pricked with a pin. Key term Pressure is exerted by a gas in terms of the collision of the molecules with the walls of the container. We know that it is fairly easy to compress gases. As the volume decreases as you compress a gas then the pressure will increase. This happens because now that the particles are closer together, they have more collisions, and as the number of collisions increases so does the pressure. Boyle’s law deals with the relationship between the two variables pressure and volume. Key term Boyle's law: The pressure of an enclosed gas is inversely proportional to the volume it occupies at constant temperature. There are several important factors to consider for Boyle’s law (as well as for the other gas laws we will be dealing with soon). The statement talks about "an enclosed gas". What is meant by an enclosed gas is that the amount of gas or the number of moles remains constant. Let’s look at some concepts that you should have dealt with in Grade 10. You learned that the mole is the SI unit for the amount of substance. Key term One mole is the amount of substance having the same number of particles as there are atoms in 12 g carbon-12. Avogadro's number is defined as the number of elementary particles (molecules, atoms, compounds, or even Coke cans for that matter) per mole of a substance. It is equal to 6,022×1023 mol-1 and is expressed as the symbol NA. It was named after Amedeo Avogadro, an Italian physicist who discovered that two gases of equal volume have the same number of molecules at the same temperature and pressure. In the early twentieth century, French scientist Jean Perrin coined the term "Avogadro's number" to describe the number of units in a mole. This is a truly large number and it is difficult to wrap our heads around really large numbers sometimes. So, to give some idea about how big the number is, if you had 1 mole of soft drink cans it would cover the surface of the Earth to a depth of over 320 km. If you were able to count atoms at the rate of 10 million per second, it would take about 2 billion years to count the atoms in one mole. This just shows that it is truly a huge number. How many grams are in one mole of water? Let’s find out. n=mM Where: n = number of moles m = mass of sample M is the molar mass of the compound Water’s formula is H2O. Hydrogen has a molar mass of 1g/mol and oxygen is 16 g/mol, so 1 mole of water is: n=mM 1=m(2×1)+16 m=18g A normal teaspoon is 5 ml or 5 g so 1 mole of water is just under 4 teaspoons of water. Hopefully, this helps you understand why we use moles to count quantities in chemistry So in Boyle’s law, remember that it is a fixed amount of gas, i.e. the amount does not change. It is called a constant variable. You might have noticed that after riding a bicycle, the tyres seem harder even though you did not pump them up more. That is because temperature can also affect the pressure of a gas. If the temperature of a gas increases the molecules move faster because they increase in kinetic energy. If they move faster, then the pressure will also increase. However, in Boyle’s law, the temperature of the gas must remain the same so it is also a constant variable. Graphing Boyle's law From the definition of Boyle’s law in the last section, we saw they have an inversely proportional relationship. Figure 2: Graph showing the inverse relationship between pressure and volume. Using the kinetic theory of gases to help explain this inverse relationship between the pressure and volume of a gas is as follows. If the volume of a gas is decreased for a fixed amount of particles, the particles are now going to collide more frequently with each other and with the sides of the container. Pressure is a measure of the number of collisions of gas particles with each other and with the sides of the container. Therefore, if the volume decreases, the number of collisions increases and so the pressure will also increase. If the volume of the gas is increased, the gas particles collide less frequently and the pressure will decrease. Boyle’s law relationship can be written as: pα1V If we used k as a proportionality constant, we could rewrite the equation as: pαkV where k is a proportionality constant. Therefore the constant k: k=p×V What this tells us is that if a gas has a constant temperature and amount of moles, then the pressure multiplied by volume will give a constant value. This gives a formula for Boyle’s law which says: p1×V1=p2×V2 Where 1 and 2 refer to readings of a fixed amount of gas at a constant temperature. Another way to graph the relationship is to consider: 1V as a variable. This would be written as; pα1V This means that the pressure is directly proportional to the inverse of the volume. Figure 3: The graph of pressure drawn against the inverse of volume. In Newton’s second law the relationship between the acceleration and mass is also inversely proportional where the acceleration always depends on the mass of the object, which means mass will be the independent variable and acceleration will be the dependent variable. However, if we use the example that we had earlier of a person squashing a balloon. Which variable, pressure or volume will be the independent variable? It will be the pressure that is causing the volume to change. The graph will still be an inversely proportional relationship but with the x and y-axis swapped around. Figure 4: Graph showing the inverse relationship between pressure and volume. The graph for volume and the inverse of pressure would be: Figure 5: Graph showing the inverse relationship between volume and the inverse of pressure. Boyle’s law is the inversely proportional relationship between pressure and volume provided the temperature of the system and the amount of particles or moles remain constant. When answering Boyle’s law, questions, or the other gas laws, read through the statement carefully to determine which law you are using. Normally in the statement, if they say the temperature remains constant then you know you must use Boyle’s law. Let’s try a few. We have already studied chemical bonding. Take a moment and see if you remember the three types of chemical bonding. Chemical bonds are the forces that keep molecules and compounds bonded together. If we want to change the chemical composition of a molecule, a chemical change needs to take place. A chemical change (chemical reaction) occurs when the composition of a substance is changed, and that requires the breaking and forming of chemical bonds during a chemical reaction. These forces (covalent, ionic and metallic bonding) are called intramolecular forces. The prefix intra- means "within’’ or inside Key term Intramolecular forces are the forces that hold atoms together within a molecule. Fun fact Interatomic (between atoms) forces are also sometimes referred to as intramolecular (within molecules) forces. A way to remember this is that you might have had inter-house athletics at school which means that the different houses competed against each other. These are the houses in the school, not competing with other schools. Covalent bonds A covalent bond forms when two atoms come close together and their half-filled orbitals overlap and the electrons are found in orbitals around both atoms. Simply put, this is when atoms share electrons to achieve a noble gas state. We use Lewis structures to show how the atoms share electrons. Covalent bonds can be single, double, or triple depending on the number of half-filled orbitals that overlap. Atoms in a single bond share two electrons, atoms in a double bond share four electrons, and atoms in a triple bond share six electrons. Key term A molecule is a particle that consists of atoms covalently bonded together. A diatomic molecule is a molecule where two of the same type of atoms are chemically bonded together. E.g. H₂, Cl2 , and O2 are all diatomic molecules. Study tip All diatomic molecules have covalent bonds. Molecules can be described as polar or nonpolar. A polar molecule is one in which there is a difference in electronegativity between the atoms in the molecule which causes the shared electron pair to spend more time closer to the atom with the higher electronegativity. This results in one end of the molecule having a slightly positive charge (+), and the other end of the molecule having a slightly negative charge (−). Therefore a polar molecule is said to be a dipole. The symbol used for a dipole is the lowercase Greek delta (δ). Figure 1: Representation of a dipole. Ionic bonds Key terms An ion is a particle with a net charge due to losing or gaining an electron. A cation is a positively charged ion. An anion is a negatively charged ion. An ionic bond is formed when there is a transfer of electrons between two atoms. This happens when the difference in electronegativity between the two atoms is greater than 1,7, which is often the case between a metal and a nonmetal. This attraction between cations and anions forms a crystal lattice where ionic bonds hold the atoms together. We don’t find individual sodium atoms attracted to individual chlorine atoms, but rather a crystal lattice of ions packed together in a 1:1 ratio. It is mostly referred to as a compound. Metallic bonds Metallic bonds occur between metal atoms. Metallic bonds are much different from the covalent and ionic bonds that we have been looking at so far. These bonds occur when metal nuclei are packed together with the valence electrons free to move among all the nuclei. These free valence electrons hold the metallic structure together. Figure 3: Metallic bonding with free valance electrons. Intermolecular forces The term “INTERmolecular forces” is used to describe the forces of attraction between molecules and ions when they are placed close to each other. The prefix inter means between. So intermolecular forces are the forces between molecules and ions. Key term Intermolecular forces are forces that exist between molecules. Intermolecular forces are much weaker than the intramolecular forces (covalent, ionic and metallic bonding) but are important because they determine the physical properties of molecules like their boiling point, melting point, density, and vapour pressure. These are NOT bonding forces. Key term Physical properties can be observed or measured without changing the composition of matter. Types of intermolecular forces Intermolecular forces are the forces that act between molecules and are responsible for the phases that substances are in. The weaker the intermolecular force, the more likely the substance will be a gas. On this page, you will see all the intermolecular forces. The type of intermolecular force will be determined by the polarity of the molecule. In previous modules, you saw that the polarity of a molecule (covalent substance) is due to the shape of the molecule and the difference in electronegativity. There are a range of different intermolecular forces. Some are stronger than others and therefore determine the effect on the properties of substances – which we will learn about in the next lesson. Ion-dipole force As the name implies, this type of intermolecular force exists between an ion and a dipole molecule. Remember when you hear the term dipole it refers to a polar molecule. A good way to understand this force is to consider what happens when you dissolve table salt (NaCl) in water (H2O). We know that there is dissociation. Key term Dissociation is the process in which solid ionic crystals are broken up into ions when dissolved in water. NaCl(s)→ Na+(aq)+ Cl-(aq) As you can see, the ionic compound is broken into positive and negative ions. The process of hydration that you learnt about in Grade 10 takes place where the water molecules surround the ions. The question is: why does that take place? Key term Hydration is the process where ions become surrounded by water molecules. There is a force of attraction between the negative ion and the positive side of the dipole (polar molecule) or the positive ion and the negative side of the dipole. This force is called the ion-dipole force. Figure 1: Ion-dipole force. If magnesium chloride (MgCl2(s)) is put into ethanol, will it dissolve? Magnesium chloride is an ionic compound and ethanol is an alcohol (which is very polar), therefore it will dissolve. To see if there is an ion-dipole force, check to see if you have an ionic compound and polar molecules. Ion-induced dipole force This is an intermolecular force that comes about between an ion and a nonpolar molecule. The word "induced" means to bring about or give rise to. When an ion approaches a nonpolar molecule, it induces polarity in the molecule by distorting the electron cloud. If you had a negative ion (anion) approach a nonpolar molecule, it would repel the electron cloud and make one side of the molecule positive. The nonpolar molecule would become a polar molecule. This leads to a weak, short-lived force which holds the compounds together. Figure 2: Ion-induced dipole force. Fun fact Ion-induced dipole forces in hemoglobin (the molecule that carries oxygen around your body). Hemoglobin has Fe2+ ions. Oxygen (O2) is attracted to these ions by ion-induced dipole forces. Key term An induced dipole is a momentary dipole in a nonpolar molecule when it attains a polarity. Here are a few examples of ion-induced dipole forces. In the presence of a nitrate ion (NO3-), the iodine molecule (I2), which is non-polar, will become a dipole. An ion-induced dipole force takes place between ions and nonpolar molecules. It is therefore important to be able to recognise if a molecule is polar or nonpolar due to its shape and electronegativity. Van der Waals forces The previous forces looked at the intermolecular forces between ions and polar and nonpolar molecules. Let’s look at forces between molecules only. A Dutch physicist Johannes Diderik van der Waals started his career as a school teacher. He became the first physics professor at the University of Amsterdam in 1877 and won the 1910 Nobel Prize in physics. His name is associated with Van der Waals forces (forces between stable molecules). There are three van de Waals forces: Dipole-Dipole forces Dipole-Induced dipole forces Induced dipole-induced dipole forces (London forces) Fun fact Geckos, insects, and some spiders have setae on the pads of their feet that allow them to climb extremely smooth surfaces such as glass. A gecko can even hang from a single toe! Scientists have found out the main reason for the adhesion, more than van der Waals forces or capillary action, is electrostatic force. Dipole-Dipole force This is the intermolecular force that exists between two polar molecules (between two dipoles). When two polar molecules come close together, they align themselves with opposite poles (positive and negative poles), and there is a force of attraction between these poles which is called a dipole-dipole force. This force can exist between different polar substances such as hydrogen bromide (HBr) and ethanol (C2H5OH). It can also exist between polar molecules of the same substance such as hydrogen bromide (HBr). Figure 4: Dipole-Dipole force between hydrogen bromide (HBr) and ethanol (C2H5OH). Figure 5: Dipole-Dipole force between hydrogen bromide (HBr) molecule. Other examples would be between HCl molecules. Why not water (H2O)? It is also polar but it is considered a special dipole-dipole force called a hydrogen bond. Hydrogen bond Hydrogen bonding is a special type of dipole-dipole attraction between molecules, not a covalent bond to a hydrogen atom. It results from the attractive force between a hydrogen atom covalently bonded to a very electronegative atom such as a N, O, or F atom and another very electronegative atom. Take note, this is not the force inside the molecule (covalent bond) but the force between molecules. Hydrogen bonds are strong intermolecular forces created when a hydrogen atom bonded to an electronegative atom approaches a nearby electronegative atom. If you consider hydrogen fluoride molecules, it is a very polar molecule due to the large difference in electronegativity. There is a hydrogen bond established between the negative fluorine side of one molecule and the positive hydrogen side of a second molecule. Figure 6: Hydrogen bond between hydrogen fluoride (HF) molecules. If you consider water molecules, it is a very polar molecule due to the large difference in electronegativity. There is a hydrogen bond established between the negative oxygen side of one molecule and the positive hydrogen side of a second molecule. Figure 7: Hydrogen bond between water (H2O) molecules. Let’s now look at ammonia molecules. They also have quite polar molecules but not as polar as with oxygen and fluorine which are more electronegative. There is a hydrogen bond established between the negative nitrogen side of one molecule and the positive hydrogen side of a second molecule. Figure 8: Hydrogen bond between ammonia (NH3) molecules. Hydrogen bonds are relatively strong intermolecular forces and substances with hydrogen will have higher boiling and melting points. A question you might ask is, why does chlorine not form a hydrogen bond if it has the same electronegativity as nitrogen? As you know chlorine is in a period below oxygen, nitrogen, and fluorine and is larger than N, F, and O. It does not make a strong H bond. Chlorine is in a lower period and therefore the size of the Cl atom is larger. The bond length is therefore greater between HCl than HF, for example, and it simply produces a dipole-dipole attraction. Dipole-Induced dipole This is the intermolecular force that exists between a polar molecule and a nonpolar molecule. When a polar molecule comes close to a nonpolar molecule there is a weak attraction between the polar molecule which induces a dipole in a nonpolar molecule by disturbing the arrangement of electrons in the non-polar molecules. Figure 9: Dipole-induced dipole between HCl and Argon Figure 10: Dipole-induced dipole between water and an oxygen molecule. To identify if you have dipole-induced dipole forces, one substance will be polar and the other will be a nonpolar molecule or atom. Induced dipole-induced dipole force or London Dispersion forces The induced-induced dipole force is the weakest intermolecular force. It is sometimes called a London dispersion force, which is the term we will use in Grade 12 while studying organic chemistry, is a temporary attractive force that results when the electrons in two adjacent atoms occupy positions that make the atoms form temporary or momentary dipoles. Due to the constant motion of the electrons, an atom or molecule can develop a temporary or a momentary dipole when its electrons are all on one side of the nuclei. Figure 11: Atoms electrons moving to one side of the nucleus producing a dipole. If another atom or molecule comes close to it in turn, it can be distorted by the dipole in the first atom or molecule. This then causes an electrostatic attraction between the two atoms or molecules called an induced - induced dipole force or London force. Figure 12: The first dipole inducing a dipole in a second atom. These forces are dominant in the halogens (e.g. F2 and I2) and other nonpolar molecules such as carbon dioxide and carbon tetrachloride. These are the weakest intermolecular forces, and therefore substances having these forces will have the lowest boiling and melting points as it requires the least energy to break these intermolecular forces. The intermolecular forces are responsible for the phases that substances are in. If the intermolecular forces are strong, then the substance's boiling and melting points will also be high. On the next page, we will go through some worked examples on intermolecular forces. What is a physical property? Key term Physical property: Any characteristic that can be determined without changing the substance's chemical identity. When a physical change takes place, it does not change the actual compound or molecules. Physical properties can be measured or observed without changing the chemical nature of the substance. A chemical change would entail changing the chemical nature of a substance through a chemical reaction. Why is knowing physical properties important? Knowing the physical properties of compounds and molecules enables scientists and engineers to use materials in different applications due to their various properties. What are the properties affected by intermolecular forces? The physical properties of melting point, boiling point, vapour pressure, evaporation, viscosity, surface tension, and solubility are related to the strength of attractive forces between molecules. The table below will help you to determine what intermolecular force exists between substances. You must be able to identify the shape as well as whether a molecule is polar or nonpolar. Figure 1: Summarising intermolecular forces. The stronger the intermolecular forces, the greater the effect it will have on the properties. We are going to study each property individually to understand the effect that the intermolecular force plays on them. If you remember from the kinetic theory of matter, the phase of a substance is dependent on the strength of the forces between its particles. The weaker the forces, the more chance the substance will be a gas. This is because the particles can move far apart since they are not held together with a strong force. If the forces are very strong, the particles are held closely together in a solid structure. In the next few pages, we will look at different physical properties such as: ❖ Vapour pressure, melting and boiling points ❖ Thermal expansion and thermal conductivity ❖ Viscosity and density ❖ Surface tension Vapour pressure Some liquids seem to change to gases more easily than others. This ease of change is called vapour pressure. Key term Vapour pressure: The pressure exerted by a vapour at equilibrium with its liquid in a closed system. The stronger the intermolecular forces, the lower the vapour pressure. Liquids with a high vapour pressure evaporate easily. Liquids with a low vapour pressure do not evaporate easily. Melting and boiling point Intermolecular forces affect the melting and boiling points of substances. Substances with weak intermolecular forces will have lower melting and boiling points than those with strong intermolecular forces, which will have high melting and boiling points. Key terms Boiling point - The temperature at which the vapour pressure of a substance equals atmospheric pressure. The stronger the intermolecular forces, the higher the boiling point. The boiling point is used in many places in industry to separate substances from each other. A process called fractional distillation is used in the production of petrol and other fuels from crude oil. What exactly is crude oil? Crude oil is a mixture of hydrocarbons (molecules made of hydrogen and carbon atoms) that exists in the liquid phase in natural underground lakes and remains liquid at atmospheric pressure. It is basically unprocessed oil. We make petrol, diesel and paraffin from crude oil, so it is quite important. Fractional distillation is a process that separates a mixture into several different parts, called fractions. Some of the hydrocarbon molecules have short molecules and need less energy to break bonds whereas some molecules have long chains and need more energy to break intermolecular forces. Crude oil is heated outside a fractional distillation column (see diagram below) until it forms mostly gases. It is cooler at the top of the column than at the bottom. As the gases rise through the fractional column, different substances condense at different temperatures. The boiling point of petrol is between 25 – 60° C but diesel fuel is 220 – 250 °C. Because they have different boiling points, they will be taken out of the fractional column at different points. This is extremely useful for us to produce the fuels we need daily. Figure 7: Fractional distillation of crude oil. In the example above, we made a liquid (component of crude oil) into a gas by heating, but can we do the opposite? To make a liquid into a gas, we must remove heat and therefore decrease the kinetic energy of the system. We are going to learn about doing the opposite now. Ammonia is a very useful substance that is used in many applications. To produce ammonia (NH3), we need nitrogen and hydrogen. The nitrogen is mostly taken from the air around us, which is a mixture of gases. So if we decrease the temperature of air, then it will form a liquid. Key term Melting point - The temperature at which the solid and liquid phases of a substance are at equilibrium. The stronger the intermolecular forces, the higher the melting point. The air in Earth's atmosphere consists of nitrogen (78 %), oxygen (21 %), argon (0,93 %) and carbon dioxide (0,038 %). Fractional distillation of liquid air. Figure 8: Fractional distillation of liquid air. By cooling air to about -200 °C, it becomes a liquid. If the temperature is slowly increased from -200 °C temperature, nitrogen gas can be taken off at -195,8 °C and oxygen gas can be removed at -183 °C. This is due to their different boiling points. What is the difference between evaporation and boiling? Evaporation occurs on the surface of a liquid. Key term Evaporation is defined as the process of conversion of liquid into vapour from the surface of the liquid at room temperature. Evaporation occurs at any temperature while boiling occurs at a fixed temperature. Thermal expansion and thermal conductivity As substances are heated, their molecules start moving more vigorously (their kinetic energy increases). This causes them to expand on heating. You can observe this in a thermometer. As the alcohol (or mercury) is heated, it expands and rises up the tube. Thermal conductivity Conduction is the transfer of thermal energy between particles that are in contact. Different materials conduct heat differently. Heat is transferred through the substance from the heated point to the other end. This is why the bottom of the pot heats up first (if you heat the pot on the stove). Metals have free, delocalised electrons that help transfer thermal energy through the metal. In covalent molecular bonds, there are no free, delocalised electrons, and heat does not pass through the material so easily. If you look at the picture below, the handles of the pot are made from plastic which is a poor thermal conductor. Viscosity and density Viscosity Some liquids flow more easily than others. Which liquid flows easier? Water, syrup or honey? The water flows much faster than the syrup or honey. Key term Viscosity is the resistance to flow of a liquid. Density From previous years, you know that in solids the atoms and molecules are arranged in an orderly way, whereas in liquids the molecules are more loosely arranged and are further apart. In gases the molecules are even further apart. These differences in arrangements of the molecules are due to the intermolecular forces between the molecules. Key term ➔ Density is a measure of the mass in a unit volume. ➔ ➔ These forces pull the molecules together which results in more molecules in one unit volume than in the liquid or gas phases. Surface tension is the property of the surface of a liquid that allows it to resist an external force, due to the cohesive nature of its molecules.What does cohesive mean? A cohesive force is the action or property of like molecules sticking together, being mutually attractive. ➔ The cohesive forces between liquid molecules at the surface do not have molecules all around it and therefore they are more strongly bound together. This forms a thin layer which makes it more difficult. ➔ The surface tension of water decreases significantly with temperature. The surface tension arises from the polar nature of the water molecule.
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