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Byju's Answer
Standard XII
Chemistry
Alcohols as Nucleophiles and Electrophiles
The reagents ...
Question
The reagents most suitable for converting primary alcohol into an aldehyde is:
A
K
2
C
r
2
O
7
and
H
2
S
O
4
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B
K
M
n
O
4
and
N
a
O
H
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C
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D
H
N
O
3
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Solution
The correct option is
C
(a)
Potassium permanganate (KMnO
4
) is a powerful oxidant able to react with primary alcohol to form carboxylic acid.
(b) Similarly, K
2
Cr
2
O
7
with H
2
SO
4
act as a strong oxidizing agent that can change primary alcohols to carboxylic acid.
(c) By using mild oxidizing agents i.e., PDC or
PCC, we can convert primary alcohols to aldehyde.
(d)
R
−
C
H
2
−
O
H
H
N
O
3
−
−−−
→
R
−
C
O
O
H
\
HNO
3
is a strong oxidizing agent; therefore it converts primary alcohol into a carboxylic acid.
Hence, the correct option is (c).
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Similar questions
Q.
Assertion (A):
C
H
3
C
H
2
O
H
can be converted into
C
H
3
C
H
O
by treatment with pyridinium chlorochromate.
Reason (R): PCC is a better reagent for oxidation of primary alcohols to aldehydes.
[1 Mark]
Q.
Name the reagent used in oxidation of a primary alcohol to aldehyde.
Q.
By which of the following reagents, both the aldehyde and the primary alcoholic group of glucose are oxidised?
Q.
Which of the following reagents can not be used to oxidise primary alcohols to aldehydes?
Q.
Show how are the following alcohols prepared by the reaction of a suitable
Grignard reagent and aldehyde/ketone?
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