ECAT Pre Engineering Chemistry Chapter 23 MCQ Test With Answer

MCQ's Test For ECAT Chemistry Chapter 23 Aldehydes and Ketones

Try The MCQ's Test For ECAT Chemistry Chapter 23 Aldehydes and Ketones

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ECAT Chemistry Chapter 23 Aldehydes and Ketones

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Question # 1

The base used in Cannizzaro's reaction is

Question # 2

A compound A has a molecular formula C2Cl3OH. It reduces Fehling solution and on oxidation produces a monocarboxylic acid B.A can also be obtained by the action of Cl2on Ethanol. A is

Question # 3

Which of the following compounds does not react with NaHSO3?

Question # 4

In aldol condensation reaction, a double bond is formed between ______ and ______ carbon atoms

Question # 5

Give IUPAC name fo Acetone

Question # 6

Formaldehyde is used to make

Question # 7

Chromyl chloride and toluene react to produce

Question # 8

Which one of the following statement is wrong regarding differences between aldehydes and ketones

Question # 9

Condensation of aldeydes withα-hydrogen gives:

Question # 10

Clemensen's reduction of ketones is carried out in

Question # 11

Calcium acetate when dry distilled gives

Question # 12

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Question # 13

Acetone is prepared by

Question # 14

The product of the reaction between propanone and HCN is hydrolysed under acidic conditions. What is the formula of the final product

Question # 15

Which reagent could be used to distinguish between CH3CH(OH)CH2CHO and CH3COCH2CH2OH

Question # 16

Which of the following is a method of converting a unsaturated ketone into unsaturated hydrocarbon?

Question # 17

Which of the following in incorrect?

Question # 18

Which of the following is halo form

Question # 19

Aledehydes ketones can be prepared form alcohols by their:

Question # 20

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Question # 21

Hydroxyl amine is a derivative of::

Question # 22

Which of the following will have the highest boiling point

Question # 23

Reduction with aluminium isopropoxide in excess of Isopropyl alcohol is called Meerwein Ponndroff-Verley reduction (MPV). What will be the final product when cyclohex-2-enone is selectively reduces in MPV reaction?

Question # 24

A compound possessingα-hydrogen atom, in the presence of dilute alkali formsβ-hydroxy aldehyde. This product on heating with dilute acid forms an unsaturated crotonaldehyde. The compound is

Question # 25

Which is not true about acetophenone?

Question # 26

Self condensation of acetaldehyde in the presence of dilute alkalies gives

Question # 27

Isopropyl alcohol on oxidation forms

Question # 28

Which of the following react with NaOH to produce an acid and an alcohol?

Question # 29

Which of the following will have the highest boiling point?

Question # 30

Reduction of aldehydes with HI and P gives

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ECAT Chemistry Chapter 23 Important MCQ's

Sr.# Question Answer
1 Iodoform test is given by:
A. Formaldehyde and Higher ketones
B. Formaldehyde
C. Acetaldehyde and methyl ketones
D. Acetaldehyde
2 A common industrial solvent is a mixture of propanone; CH3COCH3, and pentyl ethanoate CH3CO2(CH2)4CH3. Which reagent would have no effect on this solvent
A. Na(s)
B. NaBH4
C. NaOH(aq)
D. 2,4-dinitrophenylhydrazine reagent
3 Ketons are prepared by the oxidation of
A. Primary alcohol
B. Secondary alcohol
C. Tertiary alcohol
D. None of these
4 Cannizzaro's reaction in not given by
A. Formaldehyde
B. Acetaldehyde
C. Benzaldyhyde
D. Trimethylacetaldehyde
5 The product of the reaction between propanone and HCN is hydrolysed under acidic conditions. What is the formula of the final product
A. CH3CH(OH)COOH
B. CH3CH2CH(OH)COOH
C. (CH3)2C(OH)COOH
D. CH3CH2CH2COOH
6 Chromic acid used to oxidize
A. Aldehyde
B. Ketone
C. Both a and b
D. None of these
7 Which of the following is a method of converting a unsaturated ketone into unsaturated hydrocarbon?
A. Aldol condensation
B. Reimer Tiemann reaction
C. Cannizaaor's reaction
D. Wolf-kishner reduction
8 Formaldehyde is used to make
A. Plastics
B. Medicine
C. Antiseptic
D. All of these
9 Condensation of aldeydes withα-hydrogen gives:
A. Acetal
B. Ketal
C. Aldol
D. Cannizzaro product
10
Question Image
A. Treatment with HCN followed by acid hydrolysis
B. Oxidation of acetaldehyde followed by basic hydrolysis
C. Treatment with HCN followed by reduction
D. Treatment with HCN followed by oxidation

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