Question

\[C{H_3} - C \equiv CH\xrightarrow[{1\% \,HgS{O_4}}]{{40\% \,{H_2}S{O_4}}}A\]      \[\xrightarrow{\text{Isomerisation}}C{{H}_{3}}\underset{\begin{smallmatrix} \parallel \\ O \end{smallmatrix}}{\mathop{-C-}}\,C{{H}_{3}}\]
Structure of $$'A'$$ and type of isomerism in the above reaction are respectively

A. prop-1-en-2-ol, metamerism
B. prop-1-en-1-ol, tautomerism
C. prop-2-en-2-ol, geometrical isomerism
D. prop-1-en-2-ol, tautomerism  
Answer :   prop-1-en-2-ol, tautomerism
Solution :
Aldehyde and Ketone mcq solution image

Releted MCQ Question on
Organic Chemistry >> Aldehyde and Ketone

Releted Question 1

The reagent with which both acetaldehyde and acetone react easily is

A. Fehling’s reagent
B. Grignard reagent
C. Schiff’s reagent
D. Tollen’s reagent
Releted Question 2

The Cannizzaro reaction is not given by

A. trimethylacetaldehye
B. acetaldehyde
C. benzaldehyde
D. formaldehyde
Releted Question 3

The compound that will not give iodoform on treatment with alkali and iodine is :

A. acetone
B. ethanol
C. diethyl ketone
D. isopropyl alcohol
Releted Question 4

Polarisation of electrons in acrolein may be written as

A. $$\mathop {C{H_2}}\limits^{{\delta ^ - }} = CH - \mathop {CH}\limits^{{\delta ^ + }} = O$$
B. $$\mathop {C{H_2}}\limits^{{\delta ^ - }} = CH - CH = \mathop O\limits^{{\delta ^ + }} $$
C. $$\mathop {C{H_2}}\limits^{{\delta ^ - }} = \mathop {CH}\limits^{{\delta ^ + }} - CH = O$$
D. $$\mathop {C{H_2}}\limits^{{\delta ^ + }} = CH - CH = \mathop O\limits^{{\delta ^ - }} $$

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Aldehyde and Ketone


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