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Q.1 Choose The Reactant That Would Give The Product Shown

1. The reactant that would produce the product shown is option A, which undergoes an esterification reaction with methanol in the presence of an acid to form the methyl ester. 2. The product of the reaction shown is option B, which undergoes a nucleophilic substitution reaction where the amino group attacks the electrophilic carbon, displacing the methoxy group. 3. The reaction scheme least likely to be successful for the alkene is option D, which involves an oxidation reaction using osmium tetroxide that is stereospecific and would not work for this unsubstituted alkene.

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160 views1 page

Q.1 Choose The Reactant That Would Give The Product Shown

1. The reactant that would produce the product shown is option A, which undergoes an esterification reaction with methanol in the presence of an acid to form the methyl ester. 2. The product of the reaction shown is option B, which undergoes a nucleophilic substitution reaction where the amino group attacks the electrophilic carbon, displacing the methoxy group. 3. The reaction scheme least likely to be successful for the alkene is option D, which involves an oxidation reaction using osmium tetroxide that is stereospecific and would not work for this unsubstituted alkene.

Uploaded by

BHAAJI0001
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Q.

SECTION -II
PART-A
Choose the reactant that would give the product shown :

? OH

H
O

O
CH3

(A)

(B)

O
CH3

(C)

(D)

O
COOMe
2.

Predict the product of the following reaction :


CH3O

i ) H 3O
H 2 CO (
-

CH3O

(II) OH

NH2

CH3O
(A)

(B)

N-H

CH3O

MeO
MeO
(C)

(D) MeO

N-H

MeO

N
H

Choose a reaction scheme least likely to be successful for alkene (A) shown below :

(A)
O
(A)

+
+
P(Ph)3

(B)

CH 2

P(Ph)3

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