TRANSITION ELEMENTS 1 TRANSITION ELEMENTS These are large block of elements in the central position of periodic table, bridging the s-block elements at the left and p-block elements at the right (see figure next slide has the details) They are often divided into two groups, depending on the valence electrons involved in their chemistry ❑ The fist group are the d-block elements because their occurrence in the periodic table coincides with the filling of d orbitals ❑ The second group is the f-block elements, characterized by filling f-orbitals. Contained within this there are two subgroups; the lanthanides elements and the Actinides elements 2 3 This lecture focuses primarily on the d-block elements, and within this group we concentrate mainly on the elements in the fourth period or the elements of the first raw transition series , scandium (SC) to zinc (Zn) 4 Transition element is the phrase/term used to describe elements in the d and f block of the periodic table. They are termed transition because their positions in the periodic table is between the s and p block elements ❑ In the s and p blocks, elements displays strong similarities and noticeable trends across the period and down the groups of the periodic table. ❑ The same trends are observed in the d and f block elements. ❑ The first row transition elements and their electron configuration are shown in Table 1 5 Table 1: First row transition elements and their electronic configuration Element Symbol Electron configuration Sc (Z = 21) [Ar]3d14s2. Titanium Ti (Z = 22) [Ar]3d24s2. Vanadium V (Z = 23) [Ar]3d34s2. Chromium Cr (Z = 24) [Ar]3d54s1. Manganese Mn (Z = 25) [Ar]3d54s2. Iron Fe (Z = 26) [Ar]3d64s2. Cobalt Co (Z = 27) [Ar]3d74s2. Nickel Ni (Z = 28) [Ar]3d84s2. Copper Cu (Z = 29) [Ar]3d104s1. Zinc Zn (Z = 30) [Ar]3d104s2. Scandium 3d 4s 6 The term transition element and d-block elements are not sometimes the same. For example: ✓Sc (Z = 21) with an electron configuration of [Ar]3d14s2 forms Sc3+ with electron configuration of [Ar]3d04s0 in its all compounds. ✓Zn (Z = 30) with an electron configuration of [Ar]3d104s2 forms Zn2+ with electron configuration [Ar]3d10 in its compounds. ✓Copper (Z = 29) with configuration of [Ar]3d104s1 has an electron configuration of [ Ar]3d9 in its common occurring +2 oxidation State.. According to International Union and Pure Applied Chemistry (IUPAC), a transition element is defined as an element whose atom has an incomplete filled d-sub-shell or an element that give cations with incomplete filled dsub-shell. 7 According to IUPAC definition of transition elements, Scandium (Sc) and Zinc (Zn) are not strictly transition elements but are d-orbital elements because (why) they do not show characteristic features of transition elements like colored compounds and paramagnetism They have d0 or d10 configuration. Others are cadmium (Cd) and mercury (Hg). Copper with [Ar]3d104s1 electron configuration is a transition element because it has [Ar]3d94s2 electron configuration in its commonly occurring +2 Oxidation State. However, exception electron configuration is for Chromium (Z = 24) as [Ar]4s13d5 and not [Ar]4s23d4; Copper (Z = 29) as [Ar]4s13d10 and not [Ar]4s23d9 (why irregularities?) 8 Explanation This kind of irregularities is due to extra stability associated with halffilled and complete filled 3d-orbitals. For TMs forming cations, electrons are removed from the 4s orbitals than from 3d orbitals. In atoms of these transition elements, the 3d and 4s orbitals have similar energies. The 4s orbitals are conveniently described as the outer-most orbitals. This is because of the radial probability plots of the 3d and 4s orbitals (Figure 2) indicates that there is a greater probability of the 4s electrons being furthermore from the nucleus. 9 4s electrons are far from the nucleus as compared to those of 3d electrons as shown by their radial probability function or plots Figure 2. The radial probability plots of 4s and 3d 0rbitals 10 Properties of the transition elements (a) The d-block metals include elements with a wide range of properties. They encompass ➢ the most common metal used in construction and manufacturing (iron), ➢ metals valued for their beauty (gold, silver, and platinum), ➢ metals used in coins (nickel, copper, and zinc). ➢ metals used in modern technology (titanium) ➢ metals known and used in early civilizations (copper, silver, gold, and iron). 11 Properties of the transition elements (b) The d-block contains • the densest elements : Osmium, d = 22.49 g/cm3, and iridium, d = 22.41 g/cm3), ✓ the metals with the highest and lowest melting points (tungsten, MP = 3410 °C, and mercury, MP = −38.9 °C) ✓ two elements with atomic numbers less than 83 that have only radioactive isotopes [Technetium, Tc, atomic number 43; Promethium, Pm, atomic number 61, in the f -block]. 12 They have a metallic luster and conduct electricity and heat. (c) With the exception of mercury, the transition elements are solids They react with various oxidizing agents to give ionic compounds, although there is considerable variation in such reactions among the elements. They are used for jewelry and decorative items because silver, gold, and platinum resist oxidation 13 (d) Certain d-block elements are important in living organisms. ❑ Cobalt is the crucial element in vitamin B12, which is part of a catalyst essential for several biochemical reactions. ❑ Hemoglobin and myoglobin, oxygen-carrying and storage proteins, contain iron. ❑ Molybdenum and iron, together with sulfur, form the reactive portion of nitrogenase, a biological catalyst used by nitrogenfixing organisms to convert atmospheric nitrogen into ammonia (NH3) 14 (e) Many transition metal compounds are highly colored, so making them good candidates for pigments in paints and dyes Prussian blue, Fe4[Fe(CN)6]3•14H2O, This is a bluing agent used in engineering blueprint and in boundary to brighten yellowed white cloth A common pigment (artist Cd yellow) contains CdS Titanium (IV) oxide (TiO2) a whitish in most white paints 15 (f) Presence of TM cations (ions) • Crystalline silicate • Crystalline silicate Transforms them into gemstones → Fe2+ ions produces the yellow colour in citrine → Cr3+ ions produces red colour of ruby (g) TM compounds: Small quantities adds colour to glass. For example → Blue glass contains small amount of Co(II) oxide → Addition of Cr(III) oxide to glass gives a green colour 16 → Window panes and doors sometimes take on a purple color over time as a consequence of oxidation of traces of manganese (II) ion present in the glass to permanganate ion (MnO4−). Shah Mosque, Iran Basilica of St Peter and Paul 17 Importance of Transition Metals The d-block elements or metals have great importance in our daily lives. They are building blocks for life. For example: ❑ They are chief structural materials ❑ They are good electrical conductors such as silver and copper ❑ Compounds of transition elements like those of Ti, Fe and Cr are primarily constituents of paint pigments ❑ Are essential materials for photography 18 ❑ Compounds of f-block elements are used in a number of application such as ➢ colored TV screen ➢ photocopiers, ➢ efficient green emitting plasma display panels, etc. Lanthanide orthophosphate (LaPO4) doped with Cerium (Ce) or terbium (Tb) is deposited layer onto TV glass screen producing intense green Luminescence 19 Are good candidates as semiconductor materials (ZnS, ZnSe, ZnTe, CdS, CdSe, CdTe InAs etc) A device emitting in the near-IR spectral region with an external efficiency of ~0.5% based on InAs/ZnSe core-shell nanocrystals has been reported 20 Transition metal complexes plays an important role in biological processes like storage. For example Iron as TM performs many vital functions in the human body Fe is an essential trace element for human body. For example: Haemoglobin is the O-transport metalloprotein in the red blood cell Myoglobin facilitates the O2 and storage in the muscles. Cytochrome transports electrons 21 • Fe is an integral part of enzyme in various tissue. For example an average 70 kg adult body contains around 4200 mg of Fe ions (65%) The majority can be found as Haemoglobin or myoglobin which are classified as function of Fe • Fe is mainly stored in mammals as ferritin, which is essential as core of hydrated iron (III) oxide coated with protein. • The structure of Hemoglobin is as shown in the next slide 22 The structure of haemoglobin 23 24 ▪ Detoxification (a process by which a living organism converts unwanted species into harmless substance), and ▪ Structural role (metaloproteins) like the influence of zinc metal in the structure of protein-zinc insulin complexes) ▪ Plays an important roles (TMs) in polymerization process and therapeutic uses (where complexes and complexion agents are utilized to treat a variety of diseases (the aspect of medicinal chemistry-knowledge of the role of metals physiological and pathological states of the body) in the 25 ❑ TM complexes are species consisting of a transition metal coordinated or bonded to one or more ligands (neutral or anionic non metal species) and are important in catalysts, material synthesis, photochemistry and biological systems. ❑ TM complexes also display diverse chemical, optical and magnetic properties 26 Common Physical Properties of Transition Elements ➢ are metals ➢ their reactivity vary from moderate to active to inert ➢ their outermost s orbital and first d (3d) orbital of TEs comprises their valence electrons/ shells of TEs • Some or all of the electrons in s and d orbital are used when TMs forms compounds • Exhibit rich and fascinating chemistry with a variable of oxidation states and forms colored compounds due to the presence of a partially filled orbital. TMs and their compounds are useful as pigments in paints and dyes. e.g: Prussian blue (Fe[Fe(CN)6]3) is a bluing agent in laundry bleach and in engineering blue imprints 27 ❑ TM ions in crystalline silicates or alumina, such as minerals becomes gems (in Swahili vito) such as Tanzanite, Ruby etc. For example: ✓ Rubies contains Cr3+ substituted for some of the Al3+ ions in a crystal lattice of Al2O3. The TM ions gives the red color to the material and this is the reason why rubies can function as lasers ✓ Blue glasses are made by adding a small amount of Co2+ salts ✓ The green patina on copper statues and roofs is an oxidation form of copper 28 ❑ TM are hard, strong, high melting and boiling point, forms alloys with one another and with other metallic elements ❑ TM Forms colored compound with exception a few, exhibit variable oxidation state (oxidation number), d and f block elements forms array of coordination compounds. 29 ❑ TM have several oxidation states ❑ TM are often paramagnetic ❑ TM have high heat of fusion and evaporation ❑ Atomic parameters of TMs (most of them) increases across the period from left to right (For example: atomic numbers, nuclear charge increases because electrons are added to the outer shells and the nuclear charge increases due to increase of protons). ❑ TM have incompletely filled d-orbital (sub-shells) The Physical Properties of First Row Transition Elements (Fourth Period Elements are summarized in the Table (next slide) 30 Table: Electron Configuration and other Properties of the First Raw Transition Elements Electron configuration M SC TI V Cr Mn Fe Co Ni Cu Zn 4s23d1 4s23d2 4s23d3 4s13d5 4s23d5 4s23d6 4s23d7 4s23d8 4s13d10 4s23d10 M2+ - 3d2 3d3 3d4 3d5 3d6 3d7 3d8 3d9 3d10 M3+ [Ar] 3d1 3d2 3d3 3d4 3d5 3d6 3d7 3d8 3d9 EN 1.3 1.5 1.6 1.6 1.5 1.8 1.9 1.9 1.9 2 1st IE (kJ/mol) 631 658 650 652 717 759 760 736 745 906 2nd IE (kJ/mol) 1235 1309 1413 1591 1509 1561 1645 1751 1958 1733 3rd IE (kJ/mol) 2389 2650 2828 2986 3250 2956 3281 3393 3578 3833 4th IE (kJ/mol) 7130 4173 4600 4900 5020 5510 5114 5404 5683 M 162 147 134 130 135 126 125 124 128 M2+ - 90 88 85 80 77 75 69 72 M3+ 81 77 74 64 66 60 64 - - SEP (Volt) -2.03 -1.63 -1.13 -0.90 -1.18 -0.44 -0.28 -0.26 0.35 -0.763 MP (C) 1539 1668 1900 1875 1245 1536 1495 1453 1083 419 BP (C) 2730 3260 3450 2665 2150 3000 2900 2730 2595 906 3.0 4.51 6.1 7.19 7.43 7.86 8.9 8.9 8.96 7.14 31 Radius(pm) Density /gcm-3 133 - The trend in IE of the TE/TM as shown in the Table above, shows some features of transition metal chemistry. Generally, the ionization energies doubles as the oxidation states/number increases by a unit (Table above). The 4th IE of scandium shows that Sc(IV) is unlikely to occur, where as Ti(IV) and V(IV) for instance do not occur commonly. Many factors are important in determining the stability of OXIDATION STATES. Thus we cannot decide which OXIDATION STATE will occur on the basis of IONIZATION ENERGIES alone. The unipositivity of TE are not normally stable in aqueous solution because of the SIGNIFICANT SUBLIMATION ENERGY TERM in the process H SUBLIM + H HYDR + M(s) ⎯⎯ ⎯ ⎯→ M(g) ⎯⎯→ M (aq) ⎯⎯ ⎯ ⎯→ M (aq) IE 32 ❑ Metal Atomic Radius The radii of the transition elements vary over a fairly narrow range, with a small decrease to a minimum being observed around the middle of this group of elements This similarity of radii can be understood based on electron configurations. Atomic size is determined by the electrons in the outermost orbital, which for these elements is the ns orbital (n = 4, 5, or 6). Progressing from left to right in the periodic table, the size decline expected from increasing the number of protons in the nucleus is mostly canceled out by an opposing effect, repulsion from additional electrons in the (n − 1)d orbitals 33 ❑ Density The variation in metal radii causes the densities of the transition elements to first increase and then decrease across a period (Figure below). Although the overall change in radii among these elements is small, the effect is magnified because the volume is actually changing with the cube of the radius [V = (4πr3/3]. 34 The lanthanide contraction explains why elements in the sixth period have the highest densities. The relatively small radii of sixth-period transition metals, combined with the fact that their atomic masses are considerably larger than their counterparts in the fifth period, causes sixth-period metal densities to be very large. Read One result of the Lanthanide contraction is the greatest density of such as Platinum and Gold. The relative small radii of 6th period TMs combined with the fact that their mass is considerably large than their counterpart in the 5th period cause 6th period metal densities to be very large. For instance Platinum is one of the most dense metal known. Lanthanide contraction is the shrinkage of atoms following the filling of the 4f (i.e. f ) subshell (that is atoms are smaller than expected) 35 ❑ Melting and Boiling Points The melting and boiling points of any substance reflects the forces of attraction between the atoms, molecules, or ions that compose the solid. Melting and boiling points (molar enthalpy of fusion) of transition elements are very high due to strong metallic bonding in in TE (metal), which occurs due to the delocalization of electrons facilitated by the availability of both d and 2 electrons. With TEs, the MP and BP rises to a maximum around the middle of the series and then descends as shown in the pot of melting and boiling points of transition elements (see figure next slide). 36 Figure. (a) Variations of MP of 1st, 2nd and 3rd raw transition elements (b) Variation of Boiling and Melting points of First Raw (fourth period) Transition Metals/Elements The observed dip (depression) at Mn (3d5) and Zn (3d10) are caused by extra stability of half filled and full filled d-sub-shells. These electron arrangement makes them less available for contribution to the pool of metallic bonding hence weakening the metallic bond. This gives rise to the decrease of melting and boiling points. 37 ❑ Reactivity of Transition Metals Transition metals displays an increasing tendency to remain unreactive or noble. This is favored by: ✓ high heat of sublimation, ✓ high ionization energy and ✓ low heat of solvation. The high melting points suggest high heat of sublimation and the smaller the atom the greater the ionization energy (IE). The tendency is most pronounced in Platinum and Gold (underactivity) ❑ Ionization Energy The ease with which an electron may be removed from transition metal atom is intermediate between those of s and p block elements. This suggest that the transition elements (metals) are less electropositive than group 1 and 2 and may form ionic or covalent bond depending on the condition.. 38 Generally, ▪ the lower valence states are ionic ▪ higher valence states are covalent. ▪ The tendency of the ionicity decreases as the atom gets larger and the variation of ionization energies within d-block is small in all cases (lies between 5 and 10 eV ). 39 ▪ From Sc to Zn across the period small change in the first and second ionization energies are observed. Reason This is due to the build up of electrons in the immediate underlying dsub-shells that effectively shields the 4s electrons from the nucleus and minimizing the increase in effective nuclear charge from element to element. The variation of First ionization energies for First row transition elements (4th period of periodic table) are as shown in the figure below. 40 However, the increase in the THIRD and FOURTH ionization energies (table above) are rapid and the values show the usual discontinuity halfway along the series as shown in the plot of 3rd IONIZATION ENERGIES against increasing ATOMIC NUMBER (Z) of first raw transition elements (metals)This can be explained as follows: 41 The reason for the observed discontinuity is as follows: The five d-electrons are all unpaired in singly occupied orbitals. When the 6th and subsequent electrons enters, the electrons have to share (pair) the already occupied orbital resulting in inter electron –electrons repulsions, which would require less energy to remove an electron. Hence, the third ionization energy curve for the last five elements is identical in shape to the curve for the first five elements, but displaced upwards by 580 kJ mol-1 as shown in the above plot). 42 Self Assessment Question Use the values of third ionization energies of first row transition elements given elsewhere to construct a graph of ionization against first raw transition metals. Explain the reason for discontinuity observed in the trend of ionization energies between manganese (Mn) and iron (Fe) 43 ❑ Colour Many TE/TM ions and complex ions/anions containing TMs are distinctive colored . The Sc3+, V5+ and Zn2+ ions are colorless Aqueous solutions of chromium compounds with two different oxidation numbers: +3 in Cr(NO3)3 (VIOLET)) and CrCl3 (GREEN), and +6 in K2CrO4 (YELLOW) and K2Cr2O7 (ORANGE). The two Cr(III) species have different colors in solution because there are different complex ions in solution. 44 The origin of the colors of TM ions and TM compounds is due to the electronic transition involving d-orbital electrons (within partially filled d-sub-shells). As a results, this imparts colour to solid transition metal compounds and their solution. Ionic and covalent compounds of transition elements are usually colored compared to compounds of s and p block elements, which are usually white and are generally most strong reducing agents Color is associated with incomplete electron shell and the ability to promote an electron from lower energy level to higher energy level. This can be done by the absorption of light of certain wavelength . In transition elements, d-electrons are promoted to a higher energy level within the d-shell. This reflect a fairly small energy difference, the reason for the absorption in the visible region. 45 ❑ Magnetism (Magnetic Properties) Most of TRANSITION METALS and their compounds paramagnetic because they attract magnetic lines of force. pare The paramagnetic properties is associated with the presence of one or more unpaired electrons and incomplete filled d-orbitals of the metals. Other elements (substance) in which all the electron are paired do not attract lines of force and are termed diamagnetic. Recall that Fe, Co and Ni are ferromagnetic because they can be magnetized. They are unique in revealing special magnetic property hence displaying ferro-magnetism properties, the ability to be made into permanent magnets 46 ❑ Catalytic Properties Many of TMs and their compounds are excellent/good catalysts for inorganic and organic reactions including electrochemical processes. For instance, the use of vanadium pentoxide (V2O5) as catalyst in the preparation of sulphuric acid (H2SO4): How ✓ Burning of sulfur (S) in air S(s) + O2(g) ⎯→ SO2(g) ✓ Converting SO2(g) to sulfur trioxide (SO3) in the presence of V2O5 as catalyst 2SO2(g) + O2(g) V2O5 ⎯⎯→ 2SO3(g) SO3(g) + H2O(l) ⎯⎯→ H2SO4(aq) 47 The use of Platinum (Pt) as catalysts inn hydrogenation reaction 48 CHEMICAL PROPERTIES OF TRANSITION METALS Transition elements tend to be unreactive, when compared to s-block elements (i.e. they are less reactive than s-block elements). The unreactiviness tendency can be attached to: • High sublimation energy • High ionization energy • Low enthalpies of solvation In some cases, TMs are less reactive than they are supposed to be. This is due to the development of a thin protective layer on their surfaces. 49 All TMs with the exception of noble metals like Cu, Ag, Pt, Au etc., have negative electrode reduction potentials meaning that they are able or capable to react with dilute acids liberating hydrogen gas (H2). For instance: Cr(s) ⎯→ Cr3+(aq) + 3e; E = -0.90 V (OXIDATION PROCESS) 2H+(aq) + 2e ⎯→ H2(g); E = 0.00 V (REDUCTION PROCESS) Overall Reaction Cr(s) + 6H+(aq ⎯→ 2Cr3+(aq) + 3H2(g); E = -0.90 V 50 It should noted that: ✓ In normal circumstances, the forward reaction does not go unless the protective layer has been removed or dissolved. ✓ The first row transition elements/metals bearing the headed positions in their group, (refer also other head/first member of each group) are reactive metals, which undergo reaction with a very large number of elements. ✓ The chemistry of transition elements (d-block elements) have a number features which are common with the exception Sc, Zn and Cu. These features are: 51 • Oxidation States (Variable Oxidation States) This is the most striking feature of transition elements. Most of the transition metals exhibit variable oxidation states (OS) in their compounds by just loosing one or more electrons. Oxidation state (OS) is a frequently useful concept with apportions charges and electrons within the complex molecules and ions. Thus OS is a FORMAL CHARGE rather than statement of charge distribution within compounds. The OS of a metal is the formal charge, which would be placed upon that metal in a purely ionic description. For instance the metal in the gaseous phase ions M3+ and Cu+ are assigned OS of +3 and +1, respectively 52 The oxidation states of the First Row Transition Elements (4th period TMs) are shown below (shaded Oxidation States are the most common and stable while un-shaded are not stable). Sc Ti V Cr Mn Fe Co Ni Cu Zn *2 +7 *3 *6 *6 *6 *5 *5 *5 *5 +4 +4 +4 +4 +4 +4 *3 *3 *3 *3 *3 *3 *3 *2 *2 *2 *2 *2 *2 *2 *2 +1 +1 53 54 ❑ The common oxidation states for each element include +2, +3 or both. ❑ The +3 oxidation states are more stable at the beginning of the series, whereas towards the end the +2 oxidation states are more stable. The reason for this can be understood by a close examination of the IONIZATION ENERGY PLOTS 5 5 Figure. .Variation of First, Second and Third ionization energies for the first raw transition metals The variation of oxidation states (OS) can be graphically represented as shown below. • All elements displays the +1 and +2 oxidation state with the exception of SC and Zn, which forms bonding with the use of 4s electrons • From Sc to Mn there is an increase of maximum OS. This shows that for these metals, the maximum OS corresponds to both 4s electrons and all 3d – electrons 56 being used in bond formation. ❑ From Mn to Zn, the maximum OS decreases. This shows that both 4s electrons and unpaired d-orbital electrons can be used to form chemical bonds. For instance Co[Ar]3d74s2 has unpaired d electrons. So its maximum OS is +5 , 2 from 4s and 3 from 3d electrons. The above behavior of TMs is contrary to that of the s block elements, where the valency is equal to the group number and p-block elements where the valency equal to the group number or eighty (8) minus the group number. 57 ❑ The OXIDATION STATES occurs in a limited extent in the p- block, but the valence always changes by two. For instance TiCl3 and TiCl; SnCl4 and SnCl2 and PCl5 and PCl3. This is due to different causes including the INERT PAIR EFFECT. Inert pair effect is the reluctance of s-electrons to be unpaired, promoted or participate in chemical bonding. 58 Factors Influencing the Stability of the Oxidation States It is not easy to generalize the trend of stability of oxidation states of transition elements because a host of factors affecting the stability of the oxidation state. But the following factors are dominant ➢ Electronic configuration (those in the rare gas configuration are stable) ➢ The ionization energy ➢ The type of ligands ➢ Conditions of the surrounding/environment 59 Higher Oxidation States These are exhibited when the metals are in combination with fluorine ions or oxide ions. Fluorine and oxide ions are small, highly electronegative, and hence most difficulty to oxidized ions. Fluorine is often said to bring out the maximum covalency of any element. 60 Low Oxidation States • Low oxidation stated are favored by ligands that are capable of bonding by both s-donor and p -acceptor bonds. In order to do this, the ligands must posses both lone pair electrons and vacant orbitals of p-symmetry. These electrons from the ligands are donated along s-bond. 61 STUDY QUESTIONS 1. Which of the following transition metal cations are paramagnetic and which are diamagnetic?: Cr3+, V2+ Ni2+ and Cu+ 2. Identify two transition metal cations with each of the following electron configurations (use the periodic table provided to answer this question) [Ar]3d6 [Ar]3d10 [Ar]3d5. [Ar]3d8 62 3 Explain how the following properties varies in first raw transition elements (a) Ionic character (b) Basic properties (c) Ability to form variable oxidation states (d) Ability to form complexes 4. Copper with its electronic configuration [Ar]3d104s1, is included in transition elements while zinc (Zn) is not considered as transition elements. Explain 63 5(a) (b) (c) (d) What is the maximum number of unpaired d electrons that an atom or ion posses. Give an example of an atom and an ion that have this number (i) What is the lanthanide contraction? (ii) How does lanthanide contraction affect atomic size down a group of transition element (iii) How does lanthanide contraction influence the density of the elements of period 6 (i.e. 3rd raw transition elements) Explain the following (i) why are paramagnetic ions common among the transition elements but not in the main group elements (ii) Why are colored solutions are common among the transition elements, but not the main group elements Using the idea of oxidation state or oxidation number, explain the following: (i) which oxide CrO3 or CrO forms a more acidic aqueous solution (ii) Which oxide Mn2O3 or Mn2O7 displays more basic behavior (iii) Which compound does Cr exhibit greater metallic character behavior, CrF2 or CrF6. 64