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26. In a fcc lattice of X and Y, X atoms are present at the<br />

corners while Y atoms are present at the face centres.<br />

If one of the X atom from a corner is replaced by<br />

monovalent Z atom, then the formula of <strong>com</strong>pound<br />

is given as X a Y b Z. Here a is<br />

Comprehension Type<br />

Understand carefully the following two reactions and<br />

answer the questions given below :<br />

Reaction (i)<br />

NHCOCH 3<br />

Reaction (ii)<br />

Step 1 Step 2<br />

→ →<br />

CH 3<br />

Step 1<br />

→<br />

<br />

<br />

Step 2<br />

→<br />

<br />

<br />

→<br />

→<br />

NH 2<br />

SO 2 NH 2<br />

CH 3<br />

SO 2 NCl – Na +<br />

27. Which of the steps is <strong>com</strong>mon in the two<br />

reactions?<br />

(a) 1st step<br />

(b) 2nd step<br />

(c) Both the steps<br />

(d) None of the steps<br />

28. Which of the final products are medicinally<br />

important?<br />

(a) Product from reaction (i)<br />

(b) Product from reaction (ii)<br />

(c) Product from both reactions<br />

(d) None of the above<br />

Matrix Match Type<br />

29. Match the <strong>com</strong>pounds given in Column I with their<br />

shapes in Column II.<br />

Column I<br />

Column II<br />

(A) XeO 3 (P) Trigonal pyramidal<br />

(B) XeOF 4 (Q) Linear<br />

3–<br />

(C) BO 3 (R) Square pyramidal<br />

(D) I 3<br />

–(aq) (S) Trigonal planar<br />

A B C D<br />

(a) P Q R S<br />

(b) S P Q R<br />

(c) P R S Q<br />

(d) P S R Q<br />

30. Match the reactions given in Column I with the<br />

steps involved in mechanism in Column II.<br />

Column I<br />

Column II<br />

(A) Benzaldehyde reacts<br />

with methanal in<br />

presence of NaOH to<br />

give benzyl alcohol and<br />

sodium methanoate.<br />

(B) Propanone reacts<br />

with Ba(OH) 2 to<br />

form 4-hydroxy-<br />

4-methylpentan-2-one.<br />

(C) Iodoform is produced<br />

when butanone is<br />

treated with NaOI.<br />

(D) Carboxylic acids<br />

containing<br />

α-hydrogen(s) on<br />

treatment with Br 2 in<br />

presence of red P give<br />

α-haloacids.<br />

(P)<br />

Acidic<br />

nature of<br />

α-hydrogens<br />

(Q) Hydride<br />

transfer<br />

(R)<br />

(S)<br />

A B C D<br />

(a) Q, R P, Q R, S P, R<br />

(b) Q, S P, S P, R, S P, R<br />

(c) Q, S P, R, S P, R P, S<br />

(d) P, Q Q, R R, S P, S<br />

<br />

Halogenation<br />

Nucleophilic<br />

addition<br />

<br />

Keys are published in this issue. Search now! J<br />

No. of questions attempted<br />

No. of questions correct<br />

Marks scored in percentage<br />

……<br />

……<br />

……<br />

Check your score! If your score is<br />

> 90% EXCELLENT WORK ! You are well prepared to take the challenge of final exam.<br />

90-75% GOOD WORK ! You can score good in the final exam.<br />

74-60% SATISFACTORY ! You need to score more next time.<br />

< 60% NOT SATISFACTORY! Revise thoroughly and strengthen your concepts.<br />

CHEMISTRY TODAY | APRIL ‘17 57

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