INDIAN SCHOOL MUSCAT THIRD PRELIMINARY EXAMINATION CHEMISTRY ANSWER KEY

Similar documents
INDIAN SCHOOL MUSCAT THIRD PRELIMINARY EXAMINATION CHEMISTRY ANSWER KEY

CHEMISTRY MARKING SCHEME 2015 BLIND SET -56/B. Value points

Chemistry. Time Allowed: 3 hours Maximum : 70

CBSE SAMPLE PAPER

CHEMISTRY MARKING SCHEME SET -56/3 Compt. July, Value points

CHEMISTRY MARKING SCHEME SET -56/1 Compt. July, Value points

CHEMISTRY MARKING SCHEME 2015 SET -56/2/3 F. 2 3-Methylbut-2-en-1-ol 1

Organic Chemistry, 7 L. G. Wade, Jr. Chapter , Prentice Hall

CBSE Class XII Chemistry Board Paper Time: 3 Hours Total Marks: 70

voltmeter salt bridge

CHEMISTRY MARKING SCHEME OUTSIDE DELHI SET -56/2. 1 Domains are oppositely oriented and cancel out each other s magnetic moment.

Downloaded from SAMPLE PAPER-III

For more sample papers visit : CHEMISTRY. Paper 1 (THEORY) (Three Hours)

MARKING SCHEME CHEMISYRY-2015 (CODE NO. : 56/3/C)

Chemistry (Theory) [Time allowed: 3 hours] marks:70]

Downloaded from

MARKING SCHEME CHEMISYRY-2015 (CODE NO. : 56/1/C)

CHEMISTRY MARKING SCHEME OUTSIDE DELHI SET -56/1

Melting and boiling points show no definite trends in the three transition series.

M11/4/CHEMI/SPM/ENG/TZ2/XX CHEMISTRY STANDARD LEVEL PAPER 1. Monday 9 May 2011 (afternoon) 45 minutes INSTRUCTIONS TO CANDIDATES

Sample Paper Class XII Subject Chemistry

Downloaded From:

KEY ANSWERS. 1 : (a) 13:(b) 25: (a) 37: (c) 49: (b) 2 : (d) 14:(b) 26: (c) 38: (c) 50: (c)

SOLUTIONS. Dissolution of sugar in water. General Chemistry I. General Chemistry I CHAPTER

CHEMISTRY MARKING SCHEME /2/RU. NO. Value points MARKS Q.1 Due to coagulation of colloidal clay particles 1 Q.2 X 4 Y 3 1

SAMPLE PAPERS SET - I

5 2,5-Dimethylhexane -1,3-diol (CH 3 ) 2 CHCOOH < CH 3 CH(Br)CH 2 COOH < CH 3 CH 2 CH(Br)COOH Phenol (or any other correct one) 1

SOLUTIONS TO NEET ( ) - Code GG - Chemistry

CHEMISTRY PAPER 1 (THEORY)

Chemistry 12 AUGUST Course Code = CH. Student Instructions

1/2 + 1/2 Q.3 2-Hydroxy-3,3-dimethylbutanoic acid 1. Q.4 Due to +I effect of alkyl group 1

CHEMISTRY. Time : 3 Hrs. Max. Marks : 70

CHEMISTRY 1A Fall 2010 Final Exam Key

MARKING SCHEME- CHEMISTRY (043) SAMPLE PAPER (CLASS - XII)

p-block Elements Most Expected questions for CBSE Exam-2016 Structure depends on number of sum of bond pair and lone pair.

STD : 12 TH CBSE BPT 3C

CHEMISTRY. concentration of salt at equivalence point = C = 0.1 M. K = M b

MARKING SCHEME. Corresponds to the fraction of molecules that have kinetic energy. No of particles ; Tf

Unit 13-NITROGEN CONTAINING ORGANIC COMPOUNDS

WYSE Academic Challenge 2004 Sectional Chemistry Solution Set

Chapter 7: Alcohols, Phenols and Thiols

CBSE Class 12 th Chemistry Solved Guess Paper

Acid / Base Properties of Salts

(c) dilute solution of glucose (d) chloroform 12 Which one of the following represents the same net reaction as the electrolysis of aqueous H2SO4

CHEMISTRY MARKING SCHEME Guwahati SET -56/2/G. 4 Dispersed phase: Solid, Dispersion medium: Gas ½ + ½. 5 2,4 dimethylphenol 1

Name:. Correct Questions = Wrong Questions =.. Unattempt Questions = Marks =

Useful Information for Academic Challenge Chemistry Exam K = C T f = k f m

Chemistry 12. Resource Exam B. Exam Booklet

Organic Chemistry SL IB CHEMISTRY SL

Sample Paper Class XII Subject Chemistry. 3. Questions number 1 to 8 are very short answer questions and carry 1 mark each.

CH 221 Chapter Four Part II Concept Guide

CHEMISTRY PAPER 1 (THEORY)

Chapter 23 Phenols CH. 23. Nomenclature. The OH group takes precedence as the parent phenol.

NEET Set - PP

HL Topics 3 and 13 : Periodicity (2)


Chapter 17. Reactions of Aromatic Compounds

CHEM J-14 June 2014

CHEMISTRY 1A Spring 2010 Final Exam Key

For more important question's visit :

SAMPLE PAPER-1 Q 1. Q 2. Q 3. Write IUPAC name of: C 6H 5 NHCOCH 3 1. Q 4. What is Kraft temperature? 1

**The partially (-) oxygen pulls apart and surrounds the (+) cation. The partially (+) hydrogen pulls apart and surrounds the (-) anion.

Chapter 3 Acids and Bases"

Revision of Important Concepts. 1. Types of Bonding

Chemistry 2014 FOREIGN SET (56/2/1)

Chapter 4 Reactions in Aqueous Solution

FIITJEE CHEMISTRY (CBSE) CLASS 12 SOLUTION

Chemistry of Benzene: Electrophilic Aromatic Substitution

CHEMpossible. Final Exam Review

REASONING BASED QUESTIONS FROM P-BLOCK ELEMENTS GROUP-15 1 Nitrogen does not form pentahalide although it exhibit +5 oxidation state.

Chemistry 101 Chapter 4 STOICHIOMETRY

Chapter 4. The Major Classes of Chemical Reactions 4-1

Electrophilic Aromatic Substitution. Dr. Mishu Singh Department of chemistry Maharana Pratap Govt.P.G.College Hardoi

SCHOOL YEAR CH- 13 IONS IN AQUEOUS SOLUTIONS AND COLLIGATIVE PROPERTIES SUBJECT: CHEMISTRY GRADE : 11 TEST A

Analysing Acids and Bases

TEST OF CHEMISTRY. 1. 2H 2 O H 3 O + + OH, Kw = at 25 C, hence Ka is (a) (b) (c) (d)

Chapter 4. Reactions in Aqueous Solution. Lecture Presentation. John D. Bookstaver St. Charles Community College Cottleville, MO

TYPES OF CHEMICAL REACTIONS

1. A solution that is 9% by mass glucose contains 9 g of glucose in every g of solution.

CHEMISTRY. SCIENCE Paper 2

AP Chemistry. Reactions in Solution

CHEMISTRY (Theory) tt, "1 Pc. 1"1 ( oiilki&i) CLASS-XII

AP Chemistry. 4. Which atom in its ground state has the most unpaired electrons? a. Ge b. As c. Se d. Br e. Ga

There are only valence p-orbitals in N and O. Thus there is pπ-pπ bonding in oxides of nitrogen.

Ch 16 Electrophilic Aromatic Substitution

Chem 1412 Final Exam. Student:

AMINES. 3. Secondary When two hydrogen atoms are replaced by two alkyl or aryl groups.

MOCK CET TEST PAPER

Chapter 4. Types of Chemical Reactions and Solution Stoichiometry

A solution is a homogeneous mixture of two or more substances.

Chemistry STD-XII-Science-Top concepts and Notes on d and f block elements. The d and f-block Elements Top 15 Concepts

Class XII: Chemistry Chapter 13: Amines Top concepts

CHEMISTRY Midterm #2 October 26, Pb(NO 3 ) 2 + Na 2 SO 4 PbSO 4 + 2NaNO 3

15 Acids, Bases, and Salts. Lemons and limes are examples of foods that contain acidic solutions.

Please write down the Serial Number of the question before attempting it. CHEMISTRY (Theory) Time allowed : 3 hours Maximum Marks : 70

Downloaded from

I. Properties of Aqueous Solutions A) Electrolytes and Non-Electrolytes B) Predicting Solubility* II. Reactions of Ionic Compounds in Solution*

SACRED HEART COLLEGE

CHEMISTRY. PART I Answer all questionss

Transcription:

Roll Number Code Number 4 / INDIAN SCHOOL MUSCAT THIRD PRELIMINARY EXAMINATION CHEMISTRY ANSWER KEY CLASS: XII Sub. Code: 04 08.0.018 1. P type semiconductor 1. 1. (C H 5 ) N > (C H 5 ) NH > C H 5 NH > NH 1 4. 1 5. 1 6. i) The solubility of a gas in a liquid is directly proportional to the pressure of the gas at constant temperature. It is the elevation in boiling point when molality of the solution is unity. 7. i) Due to unpaired electrons in d-orbital and undergoes d-d transition. Oxygen and fluorine are strong oxidizing agents, highly electronegative and small size. i) It oxidizes iodides to iodates - MnO 4 + H O + I - MnO + OH - - + IO

It oxidizes iodide ion to iodine. MnO 4 - + 16H + + 10I - Mn + + 8H O + 5I 8. i) One S -1 i t 1/ = 0.69/k iv) slope = -k 9. i) Movement of colloidal particles towards oppositely charged electrodes under the influence of an electric field. It is a process of removal of soluble impurities from the colloid by means of diffusion through a semi- permeable membrane. 10. i) It is due to the symmetry of para-isomers that fits in the crystal better as compared to ortho and meta-isomers. Resonance effect / Difference in hybridization of carbon atom in C-X bond / Instability of phenyl cation / because of the repulsion, it is less likely for the electron rich nucleophile to approach electron rich arenes. i Alkoxide ion present in alcoholic KOH, is not only a strong nucleophile but also a strong base. 11. d = ZXM a XNa z = x (5 x 10-8 ) x 6.0 x 10 75 = r = a 4 r = x 5 4 =.165A 0 1. i) d- block elements exhibit more oxidation states because of comparable energy gap between d and s subshell whereas f-block elements have large energy gap between f and d subshell. Lanthanoid contraction. i Zn + ion has all filled orbitals whereas Cu + has d 9 (one half filled d orbital) 1. i) CO is a catalytic poison which decreases the activity of iron catalyst. The beam of light is scattered and the path of the light becomes visible. 14. i = (½) ΔT f = i K f x W B x 1000 (½)

W A x M B ΔT f = x 1.86 x 7 x 1000 (½) 100 x Δ T f = 1.1 K (1) Freezing point of solution = 7-1.1 = 71.79 K (½) 15. NH Br + i) CH COOH CH CONH CH NH + K CO + KBr + H O KOH Sn/HCl CH Cl CH NO CH NH CH NHCH Conc i Cl Cl Cl Sn/HCl HSO4 + conc HNO NO NO 16. i) van- Arkel method Reducing agent i Process of extraction of metal from the ore by reducing it at high temperature. 17. 18. k =.0 log [Ao] (½ + ½ + ½) t [A] k =.0 log 100 40 70 k =.0 x 0.155 = 0.0089min -1 40 t 1/= 0.69 (½ + ½ + ½) k t 1/ = 0.69 0.0089

t 1/ = 77.7min i) 1.5 x 10 - = k(0.1) x (0.1) y ------------- (1).0 x 10 - = k(0.) x (0.) y ------------- () 6.0 x 10 - = k(0.) x (0.4) y ------------- () Divide () by () 1 = 1 y = y y = 1 (½ ) Divide (1) by () 1 = 1 x 1 y x y x = x = 0 x = 0 (½ ) 19. rate law = k[a] 0 [B] 1 (1) 1.5 x 10 - = k(0.1) 1 (1) k = 1.5 x 10 - min -1 i) α helix- Intramolecular H bonding. β pleated-intermolecular H bonding. ( Amylose is a straight chain polymer of D glucose whereas amylopectin is a branched polymer. 0. i) [Pt(NH ) Cl(NH CH )]Cl [Ni(CN) 4 ] - dsp hybridisation, Ni in + state all electrons are paired, so diamagnetic. [Ni(CO) 4 ] sp hybridisation, Ni in 0 state all electrons are paired so diamagnetic 1. i) Bond dissociation enthalpy of S-H bond is lower than that of O-H bond. Due to small size of N than P, lone pair is readily available for donation in NH whereas in PH lone pair is delocalized due to larger size of P

i Because S-S single bond is stronger than O-O single bond.. i) Addition polymers: Polyvinyl chloride, Polythene. (½ + ½) Condensation polymers: Terylene, Bakelite. (½ + ½) Buna- N: 1,-Butadiene + Acrylonitrile. (½ + ½) Buna -S: 1,-Butadiene + Styrene. (½ + ½). i) Stable only at low temperature/ unstable at cooking temperature. (1 +1 +1 +1) Its sweetness is difficult to be controlled. i Sucralose, stable at cooking temperature and does not provide calories. iv) Protect themselves from diabetics and heart ailments 4. i) a) 4 5 b) a) Because sulphur is sterically protected by six F atoms b) Bond dissociation enthalpy of F is lower than that of Cl involved in the process. c) Bond dissociation enthalpy of HCl is lower than that of HF i) N + H NH (½) Catalyst iron (½) Promoter - K O + Al O (½) Conditions: low temperature / 700 K and high pressure (½) a) NH 4 Cl (aq.)+ NaNO (aq. ) N (g) +H O(l) +NaCl(aq.) b) P 4 + NaOH + H O NaH PO + PH i H SO 4 is a very strong acid in water because of its first ionisation to H O +. and HSO - 4. The ionization of HSO - 4 to H O + - and SO 4 is very small (it is difficult to remove a proton from a negatively charged ion).

5. i) a) The amount of substance deposited or liberated at an electrode is directly proportional to the quantity of electricity passed through the electrolytic solution. b) Molar conductivity of an electrolyte at infinite dilution can be expressed as the sum of contribution from individual ions. (1+1) Cell constant = G* = 1cm -1 5 K = 1/R x l/a ( ½ ) = 1/00 = 5 x 10 - Scm -1 ( ½ + ½) λ = 1000 x K ( ½ ) C = 5 x 10 - x 1000 ( ½ ) 0.01 = 500 Scm /mol (1) i) a) It is the conducting power of all the ions produced by dissolving 1gm mole of the electrolyte in solution. (1) b) Cells that can be recharged by passing direct current through it. (1) Ecell = E 0 cell - 0.0591 log [Sn + ] [Zn + ] (½) n [Sn 4+ ] = 0.89-0.0591 log 0.5 x (½) 1.5 = 0.8951 V (½) If [Sn 4+ ] is increased, E cell will increase. (½) 6. i) A = CH CHOHCH CH CH B = CH COCH CH CH C = CH CH CH CH CH CH CHOHCH CH CH [O Zn- CH COCH CH CH HCl 5 CH CH CH CH CH a) As Cl acts as electron withdrawing group/ CH shows +I effect. b) The carbonyl carbon atom in carboxylic acid is resonance stabalised. i) Di-tert-butyl ketone < Acetone < Acetaldehyde

a) Add neutral FeCl to both - Phenol gives a violet colour b) Add NaOH + I to both. - Acetaldehyde yellow ppt of iodoform i a) b)