KENDRIYA - VIDYALAYA BASTI PRE-BOARD I 2015-16 BLUE PRINT (XII CHEM) S.NO UNIT VSA (1 mark) SA I (2 marks) SA II VBQ LA (3 marks) (4 marks) (5 marks) 4(2) Total 1 Soild State 4(2) 2 Solutions 3 Electrochemistry 2(1) 3(1) 5(2) 4 Chemical Kinetics 2(1) 3(1) 5(1) 5 Surface Chemistry 3(1) 4(1) 6 General principles and processes 3(1) 3(1) 6(2) 8(3) 5(1) 1(1) 5(1) of Isolation of Elements 7 p -Block Elements 2(1) 8 d- and f-Block Elements 9 Coordination Compounds 10 Haloalkanes and Haloarenes 11 Alcohols, Phenols and Ethers 12 Aldehydes, Ketones and Carboxylic Acids 1(1) 13 Organic Compounds Containing 1(1) 3(1) 4(2) 1(1) 3(1) 4(2) 1(5) 1(1) 5(1) 3(1) 3(1) 3(1) 4(2) 3(1) 3(1) 1(5) 6(2) Nitrogen 14 Biomolecules 15 Polymers 16 Chemistry in Everyday Life Total 4(1) 4(1) 3(1) 5(5) 10(5) 36(12) 3(1) 4(1) 15(3) 70(26) KENDRIYA VIDYALAYA BASTI PRE-BOARD I 2015-16 CLASS: XII SUBJECT: CHEMISTRY (Theory) MARKING-SCHEME Q. no. Value- points Mar ks 1 A bond formed between -NH2 group of one carboxylic acid & -COOH group of other carboxylic acid. 1 1 2 NH3 , because it has higher critical temperature. ½ +1/2 1 1 1 1 1 3 4 Because of long hydrocarbon part, which is hydrophobic in nature hexanoic acid is slightly soluble in water. 5 N-methyl propanamide. 6 For FCC, Z =4 1 1 ½ Density of cell= 7.2 gcm-3 , a = 288pm = 2.88 x 10-8cm d= Z x M/a3 x NA ½ M = (d x a3 x NA)/Z 7 8 = 7.2 x (2.88 x 10-8)3x 6.022 x 1023/4 ½ = 25.9gmol-1 ½ (a) PCl3 + 3H2O H3PO3 + 3HCl (b) XeF6 +H2O XeOF4 + 2HF 1 1 At anode 2Fe(s) --- 2Fe2+ + 4e- ½ At cathode O2(g) +4H+ (aq) + 4e- -- H2O(l) ½ 2 2 The overall reaction: 2Fe(s) + O2(g) +4H+ (aq) ) --- 2Fe2+ + H2O(l) 1 2 9 10 a. b. a. b. i-Frenkel defect ii-Both Shottky & Frenkel defect Decreases. Rate of reaction becomes 4 times. Rate of reaction becomes 1/4 times. 1 1 1 1 2 OR The reactions which are not truly of the first order but under certain conditions behave as first order. 1 H+ C12H22O11 + H2O -- C6H12O6 + C6H12O6 Sucrose glucose fructose 11 12 1 2 a. Amino acids may be acidic, basic or neutral depending upon the relative number of amino and carboxyl group. Equal no. of amino and carboxyl group = Neutral More amino gp =Basic More carboxyl gp = Acidic b. The sugar having –CHO groupso can redce Tollen’s & Fehling’s reagent. E.g glucose (any one example) a)Correct order b) Correct reaction ½ ½ ½ ½ 1 3 1 1 1 c) Correct reason 3 13 1 Benzoyl peroxide CH3-CH=CH2 + Br2 ------------- CH3-CH2-CH2Br ii) Due to following reasons: 1 -Double bond character of C-X bond in haloarenes. - More electronegative nature of carbon(sp2 hybridised ) to which halogen is bonded in Haloarene. 1 Any other correct reason 3 14 Antiseptic Disinfectant 1. These are antibacterial agents These are antibacterial agents which which prevent the growth of kill the micro organisms . And are micro organisms or may even applied to inanimate objects. kill them. And are applied on wounds. 2. Eg. Chloroxylenol. (or any Eg. 1% Phenol solution. other correct example) b. To impart antiseptic properties in soaps. 1+1 1 OR a. Antacids: The substances which neutralize the excess acid and raise the pH to an Appropriate level in stomach are called antacids. eg. Mixture of aluminium and magnesium hydroxide. b. Antifertility drug: These drugs are used to check pregnancy in women. For eg. Norethindrone. 1 1 c. 15 Antioxidants: An antioxidant is a molecule that inhibits the oxidation of other molecules. Oxidation reactions can produce free radicals. In turn, these radicals can start chain reactions. When the chain reaction occurs in a cell, it can cause damage or death to the cell. Antioxidants terminate these chain reactions by removing free radical intermediates, and inhibit other oxidation reactions. For eg. Butylated hydroxyl toluene(BHT ) i) For solution I Λm = k/ c k= 1 1 3 ½ ρ ½ 3 -1 Λm= 1x 1000 = 1 x 1000 cm L ρ c 58 Ωcm x 0.20mol L-1 ½ Λm = 86.2 Ω-1cm2mol-1 ii) For solution II Λm= k x 1000 = 2.5 x 10-2 Ω-1cm-1x 1000 c 0.20mol L-1 ½ ½ -1 2 -1 Λm = 125 Ω cm mol ½ Solution II will have larger molar conductivity. 16 For first order reaction k = 0.693= ½ 0.693 t1/2 4 hr ½ t = 2.303 x log [R]0 [R] k ½ log [R]0= k x t [R]2.303 ½ log [R]0 = 0.693x 7 = 4.851 [R]2.303 x 4 9.212 ½ 0 Log[R] = 0.5266 [R][R] ½ = 3.362 [R]0= 1M [R] = 3.362 [R] = Antilog 0.5266 0 [R]0___ 3 = 1/3.362 = 0.2974M After 7 hrs Sucrose left = 0.2974M 3 17 18 a) Due to high bond energy of p∏- p∏bond between nitrogen atoms. b) The bond energy of H2S bond is more than that of H2Te bond. c) Due to small size of fluorine and more hydration enthalpy. White phosphorous 1. It is insoluble in carbon disulphide. 2. It is less stable as compared to red phosphorous due to the angular strain. Red phosphorous 1 1 1 1+1 It is soluble in carbon disulphide. More stable than White phosphorous. 1 b) Chlorine water is yellow due to presence of hypochlorousacid(HClO). On standing HClO being unstable it decomposes to form HCl. 19 20 21 a) Tyndall-effect occurs. b) Coagulation of the sol takes place. c) Electrophoresis occurs. a) The role of NaCN is to dissolve the gold to form aurocynide complex. The metal is obtained by displacement from this complex. 4Au + 8NaCN + 2H2O + O2 ----- 4Na[Au(CN)2] + 4NaOH b) The role of silica is to remove the iron oxide (obtained during the oxidation) ∆ FeO + SiO2 --------------- FeSiO3 (slag) c) Iodine forms a compound with Zirconium at decomposes further to give pure metal. ∆ Zr(impure) + 2I2 ------ ZrI4 ∆ ZrI4 ---------Zr(pure) + 2I2 a) +3 Oxidation state. b) d2sp3 c) Octahedral d) Paramagnetic e)Potassium hexacyanatoferrate(III) ion f) [Fe(CN)6]3- 22 23 a) i) DNA ii) RNA b) Vitamin K c) β – D – Galactose 3 3 1 1 1 ½ ½ ½ ½ 1/2 1/2 3 ½ ½ ½ ½ ½ ½ 3 and β – D – Glucose a) Because they are not biodegradable. b) These can be easily recycled and coloured polythene contain lot of poisonous substances. c) Ethene d) Care and concern towards environment, public awareness etc. ½+½ 1 ½+½ 1 1 1 1 3 4 24 a) Depression in freezing point will be same, because both are non electrolytes and give same number of solute particles. (in moles) b) ∆Tf = Kf x Wsolute x 1000 Msolute x Wsolvent 1+1 1 1.8 = 1.86 x Wsolute x 1000 ½ 1000 x 74.5 ½ Wsolute = 1.8 x 74.5 1.86 1 Wsolute = 72.09 g OR a) If Pressure applied on the solution should is larger than the osmotic pressure , the process of reverse osmosis occurs. b) i = 3 c) Relative lowering in vapour pressure = p10- p1= x2 p10 1 1 ½ = p10- p1= W2 x M1 p10M2 x W1 ½ 1.013 – 1.004 = 2 x 18 1.013 M2 x 98 M2 = 1.013 x 2 x 18 1 0.009 x 98 M2= 41.35 g mol-1 25 a) Because of tendency of oxygen to form double bond with transition metals. b) Electronic configuration of Mn2+ is 3d5which is half filled hence stable, hence IIIrd ionisation enthalpy is very high. In case of Fe2+ electronic configuration is 3d6. Hence it can lose one electron easily to give more stable configuration 3d5. c) This is due to poor shielding by 5f electrons in the actinides than that by 4f electrons in the lanthanoids. d) i) Cr2O72- +14H+ + 6I- 2Cr3+ + 3I2 + 7H2O ii) MnO4- + 8H+ + 5Fe2+ Mn2+ + H2O + 5Fe3+ OR a) In aqueous solution: Cr2O72- + H2O ↔ 2CrO42- + 2H+ Dichromate ion Chromate ion (Orange Red) (Yellow) In Acidic medium (i.e decreasing pH) equilibrium shifts towards backwards and the colour is orange red. Whereas in basic medium equilibrium will shift forward and the solution is yellow. 1 5 1 1 1 1 1 1 1 b) i) Because of d-d transition. ii) Due to their ability to to adopt multiple oxidation state and to form complexes. iii) Europium (II) has stable electronic configuration (half filled) ie [Xe] 4f7 5d06s0. 26 a) i) Ethanal gives iodoform test whereas propanal does not. CH3CHO + 3NaOI HCOONa + CHI3 + 2NaOH Ethanol iodoform (Yellow ppt.) ii) Phenol and benzoic acid can be distinguished by ferric chloride test. 6C6H5OH + FeCl3Iron phenol complex (Violet colour) 1 1 1 5 1 1 3C6H5COOH + FeCl3 Ferric benzoate (Pale brown ppt.) (b) (i) 2HCHO + Conc.KOH ------ CH3OH + HCOOK H2O 1 1 (ii) CH3CH2CHO + CH3MgBr -------- CH3CH2CH(CH3)(OH) CO, HCl (iii) C6H6 ------- C6H5CHO 1 OR (a) 1 (i) 1 (ii) (b) i) Because in carboxylic acids the hydrogen bonding is much stronger than that in alcohols, so they have high boiling points. ii) In Chloroacetic acid, the -Cl shows –I effect and hence creates less electron density on the oxygen of carboxylic acid thus the release of proton becomes easier. iii) Butanone < Propanone <Propanal<Ethanal. -------------------------------------------------------------------- 1 1 1 5