Reaction Mechanism MCQ -1 (Advanced)


15 Questions MCQ Test Chemistry for JEE Advanced | Reaction Mechanism MCQ -1 (Advanced)


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This mock test of Reaction Mechanism MCQ -1 (Advanced) for JEE helps you for every JEE entrance exam. This contains 15 Multiple Choice Questions for JEE Reaction Mechanism MCQ -1 (Advanced) (mcq) to study with solutions a complete question bank. The solved questions answers in this Reaction Mechanism MCQ -1 (Advanced) quiz give you a good mix of easy questions and tough questions. JEE students definitely take this Reaction Mechanism MCQ -1 (Advanced) exercise for a better result in the exam. You can find other Reaction Mechanism MCQ -1 (Advanced) extra questions, long questions & short questions for JEE on EduRev as well by searching above.
*Multiple options can be correct
QUESTION: 1

The  correct statement(s) about solvent effect is\are :

Solution:

Solvent effect.

*Multiple options can be correct
QUESTION: 2

Which of the following reaction(s) is\are posible

Solution:
*Multiple options can be correct
QUESTION: 3

Solution:

*Multiple options can be correct
QUESTION: 4

Solution:
*Multiple options can be correct
QUESTION: 5

Which of the following reaction will go faster if the concentration of the nucleophile is increased?

Solution:
QUESTION: 6

 Identify the one which on reaction with carboxylic acid at high temperature gives Ester

Solution:

 Alcohols on reaction with carboxylic acid at high temperature, in the presence of sulphuric acid gives Ester.

QUESTION: 7

Solution:
QUESTION: 8

. In the following reaction sequence, what will be X?

Solution:

Aniline will be X as we can see below reaction. Free bromination will occur, and bromine will get add to ortho and para position followed diazotisation and a rapid reaction will take place between diazonium ion and C2H5OH and 1, 3, 5-tribromo benzene will form.

QUESTION: 9

 What will be the (X) in the below mentioned reaction sequence?

Solution:

As we can see in below reaction, that firstly diazotisation reaction will occur. This is followed by reaction of NaNO2 1 with diazonium ion forming nitro benzene, which will undergo reduction and form aniline.

QUESTION: 10

Compound W is

Solution:

QUESTION: 11

Compound 'X' is

Solution:

QUESTION: 12

Match the column I with column II

Solution:
QUESTION: 13

Solution:
QUESTION: 14

Correct statement about nucleophiles and leaving groups is/are

Solution:
QUESTION: 15

Which intermediate is involved in the reaction given below?

Solution:

As we can see, in first step in presence to light carbene is formed.

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