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Aldehydes, Ketones and Carboxylic Acids · Question 49

AIPMT 2012 (Prelims)MCQEasy📈 Topic in 12% papers+4−1
1

CH3CHO and C6H5CH2CHO can be distinguished chemically by

  1. Benedict's test
  2. Iodoform test
  3. Tollens' reagent test
  4. Fehling's solution test

Answer

(2) Iodoform test

Solution

Both are aldehydes with α-hydrogens, so both reduce Tollens' reagent, Fehling's solution and Benedict's solution.

As per NCERT, compounds having a CH3CO- group (methyl ketones and acetaldehyde) give the iodoform test.

CH3CHO+3I2+4NaOH CHI3 (yellow)+HCOONa+3NaI+3H2O

C6H5CH2CHO has no CH3CO- group no iodoform.

Answer: (2)

AIPMT 2012 (Prelims)

Keep practising — Aldehydes, Ketones and Carboxylic Acids

2

The correct order of decreasing acid strength of trichloroacetic acid (A), trifluoroacetic acid (B), acetic acid (C) and formic acid (D) is

  1. B > A > D > C
  2. B > D > C > A
  3. A > B > C > D
  4. A > C > B > D
AIPMT 2012 (Prelims)
3

Predict the products in the given reaction. [figure]

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
AIPMT 2012 (Prelims)
4

Acetone is treated with excess of ethanol in the presence of hydrochloric acid. The product obtained is

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
AIPMT 2012 (Prelims)
5

The order of reactivity of phenyl magnesium bromide (PhMgBr) with the following compounds: [figure]

  1. III > II > I
  2. II > I > III
  3. I > III > II
  4. I > II > III
AIPMT 2011 (Mains)
6

Clemmensen reduction of a ketone is carried out in the presence of which of the following?

  1. Glycol with KOH
  2. Zn-Hg with HCl
  3. LiAlH4
  4. H2 and Pt as catalyst
AIPMT 2011 (Prelims)
7

Following compounds are given (i) CH3CH2OH (ii) CH3COCH3 (iii) CH3- CH3 |CHOH (iv) CH3OH Which of the above compound(s), on being warmed with iodine solution and NaOH, will give iodoform?

  1. (i), (iii) and (iv)
  2. Only (ii)
  3. (i), (ii) and (iii)
  4. (i) and (ii)
AIPMT 2010 (Mains)
8

Which one of the following compounds will be most readily dehydrated?

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
AIPMT 2010 (Mains)
9

In a set of reactions, ethylbenzene yielded a product D. [figure] D would be

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
AIPMT 2010 (Prelims)
10

Which of the following reactions will not result in the formation of carbon-carbon bonds?

  1. Reimer-Tiemann reaction
  2. Cannizzaro reaction
  3. Wurtz reaction
  4. Friedel-Crafts acylation
AIPMT 2010 (Prelims)
11

Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is

  1. CH3COOCH3
  2. CH3CONH2
  3. CH3COOCOCH3
  4. CH3COCl
AIPMT 2010 (Prelims)

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