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The enol form of acetone, after treatment with D2O gives

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Important Questions on Aldehydes, Ketones and Carboxylic Acids

HARD

Consider the reactions:

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Identify A, X, Y and Z.

MEDIUM
Which of the following reagents would distinguish cis-cyclopenta-1, 2-diol from the trans-isomer?
EASY
Aldehydes or ketones when treated with C6H5-NH-NH2, the product formed is
MEDIUM
Which is the main organic product obtained by the reaction of 2, 2, 2 trichloro ethanal with calcium hydroxide?
MEDIUM
Which of the product is formed when acetone is reacted with barium hydroxide solution?
MEDIUM

Represent the union of two sets by Venn diagram for each of the following.

X={x | x is a prime number between 80 and 100}

Y={y | y is an odd number between 90 and 100}

HARD
The product formed by Claisen - Schmidt reaction of (A) and (B) is:

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MEDIUM
Acetylene and HCHO react in presence of copper acetylide catalyst to form
HARD
A keto ester (A) with molecular formula C6H10O3 on treatment with NaOH+I2 does not give iodoform but on boiling with dilute KOH gives a compound (B) with molecular formula C4H5O3K which upon acidification followed by heating undergoes decarboxylation to give acetone. The keto ester (A) is
HARD
Aldehydes can undergo aldol condensations and Cannizzaro reactions depending upon the reaction conditions.
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