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+2 NEET IntelliQuest PCB-3 (28.01.2021) AnsKey - 10645292

This document contains the answer key for a chemistry exam targeting NEET 2021. It provides answers to 45 multiple choice questions testing various chemistry concepts. The answers are explained concisely, with key steps and reasoning provided. Reactions and mechanisms are depicted using chemical structures and symbols. The document is organized with chemistry questions grouped together, followed by questions testing physics and biology.

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0% found this document useful (0 votes)
25 views

+2 NEET IntelliQuest PCB-3 (28.01.2021) AnsKey - 10645292

This document contains the answer key for a chemistry exam targeting NEET 2021. It provides answers to 45 multiple choice questions testing various chemistry concepts. The answers are explained concisely, with key steps and reasoning provided. Reactions and mechanisms are depicted using chemical structures and symbols. The document is organized with chemistry questions grouped together, followed by questions testing physics and biology.

Uploaded by

swap2005sharma
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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XII/IQM#3/28/01/2021/PCB Ans.

Key Target NEET 2021

CHEMISTRY
1. A
Sol. 2nd step is oxidative ozonolysis which give acid.
2. C
1
Sol. Heat of hydrogenation 
hyperconjugation
Heat of hydrogenation of cis > trans.
3. C
H
H2SO4 O3
CH2 O + O C
 Zn – H2O H
OH
Sol. A Decolourise cold KMnO4
resist oxidation
4. C
5. C

Sol.
sp  Non planar.
2
N

H H
6. C 7. C
8. B
Sol. It has 3 acidic hydrogen & will produce 1.5 mol H2
9. B 10. C
11. B
Sol. Electron withdrawing gp on substrate is excellent substrate for SN2
12. A 13. A
14. A H
B2H6 PCC
Sol. H3C – CH2 – C= CH2 H2O2/HO
– CH3CH2 – C – CH2OH CH3CH2 – CH – CHO
CH3 CH3 CH3
(X) (y) Chiral
OH O
| ||
If X is CH 3  CH  C  CH 3  CH 3  CH  CH  CH 3  CH 3  C  CH  CH 3 (Inactive )
| | |
CH3 CH3 CH3
15. B
Sol. sp2 hybridisation is very less stable at bridgehead carbon of a bicyclic compound.
16. A 17. A
18. B
CH2 CH2
+ CH2 +
H -H
OH 
Sol. -H2O

19. C
Sol. It is 3° alcohol that gives 3° carbocation which is easily formed.

Page #1
XII/IQM#3/28/01/2021/PCB Ans. Key Target NEET 2021
20. B

Sol. In CH 3 CO C H2CH 2Br , the -hydrogen is more acidic due to electron-withdrawing effect of the C = O
group, therefore, it can be easily abstracted by a base. Further, the product formed is stabilized by
resonance due to conjugation of the double bond with the C = O group. Thus CH3COCH2CH2Br is most
reactive towards alcoholic KOH

CH 3 COCH 2 CH 2Br    CH 3  C  CH  CH 2  CH 3  C  CH  C H2
KOH( alc .)
 HBr || |
O O
21. A
  
H2O
Sol. C 6H5  C H  OCH 3   C 6H5  C H  O CH 3  C 6H5  CH  O CH 3
|  Highly stabilise
Cl
22. D
Sol. Carbocation rearrangement as Benzylic carbocation is more stable
23. A
CH3 CH3 O OH
||
| | |
Sol. CH3  CH  Br  Mg 1. C6H5  C  CH3
 CH3  CH  Mg  Br 
 CH3  C  C6H5
2. H2O |
CH  CH3
|
CH3
24. B 25. A 26. B O O
27. D COCH3 COO Na
– +

Sol. Aralkyl halides are more reactive than aryl NaOI


halides, therefore, only the halogen in the side Sol. iodoform
+ CHI3
chain is displaced. +
H
CH2Cl CH2CN
NaCN OH O
DMF COOH COOH
NaBH4
I I water
28. D
Sol. It is SN2 & aprotic polar solvent will favour. 39. C
29. B 40. D
30. A Sol. NaBH4 will not reduce double bond
Sol. It is SN2 attack of CH3O–, on less hindered side 41. B
Sol. A = CH3CN; B = CH3COOH; C = CH3CH2OH
CH3 3 OCH3
2 42. A
to form 1 43. A
OH
Sol. X is cis and Br2 has anti-attack. The product has
to be a racemic mixture
31. B 32. C 33. C Y is trans and anti-attack of Br2 gives meso
34. A compound i.e., C and D are same compound
35. B 44. B
CH3 CCl3 CCl3
Sol. Li
+
Li 3Cl2/ Br2/Fe
Br Sol.
Sunlight
D2O Br

45. C
D
36. B 37. C
38. A

Page #2
XII/IQM#3/28/01/2021/PCB Ans. Key Target NEET 2021

Physics and Biology (Answer Key)

Page #3

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