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Aldehydes, Ketones and Carboxylic Acids · Question 52

AIPMT 2012 (Prelims)MCQEasy📈 Topic in 38% papers+4−1
1

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]

Answer

(4) [figure]

Solution

As per NCERT, ketones react with alcohols in the presence of dry HCl gas to form a hemiketal first and then a ketal (with excess alcohol).

(CH3)2C=O [dry HCl]C2H5OH(CH3)2C(OH)OC2H5 [dry HCl]C2H5OH(CH3)2C(OC2H5)2+H2O

With excess ethanol the product is the ketal, 2,2-diethoxypropane.

Answer: (4)

AIPMT 2012 (Prelims)

Keep practising — Aldehydes, Ketones and Carboxylic Acids

2

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)
3

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)
4

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)
5

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

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
AIPMT 2010 (Mains)
6

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)
7

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)
8

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)
9

Propionic acid with Br2/P yields a dibromo product. Its structure would be

  1. [figure]
  2. CH2(Br)-CH2-COBr
  3. [figure]
  4. CH2(Br)-CH(Br)-COOH
AIPMT 2009
10

A strong base can abstract an α-hydrogen from

  1. ketone
  2. alkane
  3. alkene
  4. amine
AIPMT 2008
11

The relative reactivities of acyl compounds towards nucleophilic substitution are in the order of

  1. Acid anhydride > Amide > Ester > Acyl chloride
  2. Acyl chloride > Ester > Acid anhydride > Amide
  3. Acyl chloride > Acid anhydride > Ester > Amide
  4. Ester > Acyl chloride > Amide > Acid anhydride.
AIPMT 2008

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