Reactive Inter & Reaction Mechanism


20 Questions MCQ Test GATE Chemistry Mock Test Series | Reactive Inter & Reaction Mechanism


Description
This mock test of Reactive Inter & Reaction Mechanism for Chemistry helps you for every Chemistry entrance exam. This contains 20 Multiple Choice Questions for Chemistry Reactive Inter & Reaction Mechanism (mcq) to study with solutions a complete question bank. The solved questions answers in this Reactive Inter & Reaction Mechanism quiz give you a good mix of easy questions and tough questions. Chemistry students definitely take this Reactive Inter & Reaction Mechanism exercise for a better result in the exam. You can find other Reactive Inter & Reaction Mechanism extra questions, long questions & short questions for Chemistry on EduRev as well by searching above.
QUESTION: 1

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QUESTION: 2

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QUESTION: 3

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QUESTION: 4

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This reaction is stereoselective, co-ordination of the oxygen atom to the sinc.

QUESTION: 5


The major product of the reaction is

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QUESTION: 6

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*Answer can only contain numeric values
QUESTION: 7

 

How many monochlorinated products are possible including stereoisomer?


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QUESTION: 8

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QUESTION: 9

Product formed in the above reaction, which of the following correct mechanism apply

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This reaction mechanism proceed through addition elimination

QUESTION: 10

 

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QUESTION: 11

The reaction of the bromo compound shown below with sodium ethoxide gives predominantly

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Chemical transformation involved in above chemical reaction can be illustrated as

QUESTION: 12

The major product obtained in the reaction below is

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*Answer can only contain numeric values
QUESTION: 13

The total number of compounds (shown below) that form phenylhydrazone derivatives under acidic conditions is ____________





 


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From the above compound, five compound form phenylhydrozone derivative under acidic condition.

*Answer can only contain numeric values
QUESTION: 14

How many product will be formed the following reaction is


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QUESTION: 15


Correct product (Q, R and P) in the above reactions are formed respectively

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QUESTION: 16

The major product (P) in the above reaction is 

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QUESTION: 17

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QUESTION: 18

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Oxidation of the allylic alcohol using the chiral ligand (+) di-isopropyl tartrate, the (S) enantiomer reacts about a hundred times faster than the (R) enantiomers epoxide formed from less hindered side.

QUESTION: 19

Which of the following statement(s) is true about the reaction given below?

(1) it involves a carbocation intermediate
(2) rearrangement is due to SN1 reaction mechanism.
(3) it proceeds via a concerted SN2 pathway
(4) it involves neighbouring group participation.

Solution:


From above mechanism:
If proceecs via a concerted SN2 pathway.
It involves neighbouring group participation.

QUESTION: 20

Solution:

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