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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