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Assignment for Class 12 Chemistry Unit 12 Aldehydes, Ketones And Carboxylic Acids
Class 12 Chemistry students should refer to the following printable assignment in Pdf for Unit 12 Aldehydes, Ketones And Carboxylic Acids in Class 12. This test paper with questions and answers for Class 12 Chemistry will be very useful for exams and help you to score good marks
Unit 12 Aldehydes, Ketones And Carboxylic Acids Class 12 Chemistry Assignment
Question: Carbonyl compounds are the constituents of
(a) fabrics
(b) flavouring
(c) plastics and drugs
(d) All of these
Answer: d
Question: The bond angle and structure of carbonyl compounds respectively are
(a) 120° and trigonal planar
(b) 109°28' and tetrahedral
(c) 120° and tetrahedral
(d) 109°28' and trigonal planar
Answer: a
Question: Which of the following substrates give the same product on the reduction with DIBAL-H?
(a) CH3 — (CH2)9— CN and CH3(CH2)9 — COOH
(b) CH3 — (CH2)9— CN3and CH3(CH2)9 — COOC2H5
(c) CH3 — (CH2)9 — COOH and CH3 (CH2)9 — CHO
(d) CH3 (CH2)9 —COOH and CH3(CH2)9 COOC2H5
Answer: b
Question: The name of simplest aromatic aldehyde carrying the aldehyde group on a benzene ring is/are
(a) carbaldehyde
(b) benzene carbaldehyde
(c) benzaldehyde
(d) Both (b) and (c)
Answer: d
Question: The most suitable reagent for the conversion of R—CH2—OH→R—CHO is
(a) KMnO4
(b) K2Cr2O7
(c) H2SO4
(d) PCC (pyridinium chlorochromate)
Answer: d
Question: The compounds methanal, ethanal and propanone are miscible with water because they form
(a) van der Waals’ forces with water
(b) ‘H’-bonding with water
(c) dipole-dipole bond with water
(d) ion-dipole bond with water
Answer: b
Question: Name the product formed during the decarboxylation of malonic acid.
(a) Acetic acid
(b) Ethanone
(c) Propanone
(d) Formic acid
Answer: a
Question: Identify the example in which nucleophilic addition followed by elimination reaction occur respectively in the carbonyl compound.
(a) Addition of Grignard reagent
(b) Addition of sodium sulphide
(c) Addition of HCN
(d) Addition of NH3
Answer: d
Question: Alcohol vapours are passed over which of the following catalysts to give aldehydes and ketones?
(a) S or Pd
(b) Ag or Cu
(c) F or Cl
(d) Li or K
Answer: b
Question: Which of the following compounds produces an orange-red precipitate with 2, 4-DNP reagent?
(a) Acetamide
(b) Dimethyl ether
(c) Butanone
(d) Propylbutanoate
Answer: c
Question: Some higher members of aliphatic carboxylic acids known as fatty acids occur in natural fats as esters of glycerol. How many C-atoms do they contain?
(a) C12-C18
(b) C10-C15
(c) C5-C10
(d) C20-C30
Answer: a
Question: Select the acid(s) which cannot be prepared by Grignard reagent?
(a) Acetic acid
(b) Succinic acid
(c) Formic acid
(d) All of these
Answer: a
Question: On heating an aldehyde with Fehling’s reagent, a reddish brown precipitate is obtained due to the formation of
(a) CuO
(b) Cu2O
(c) CuSO4
(d) Cu2++O−H
Answer: b
Question: Carboxylic acids have higher boiling points than aldehydes, ketones and even alcohols of comparable molecular mass. It is due to
(a) more extensive association of carboxylic acid via van der Waals’ force of attraction
(b) formation of carboxylate ion
(c) formation of intramolecular H-bonding
(d) formation of intermolecular H-bonding
Answer: d
Question: Which of the following reagents is/are used for the conversion of ethanoic acid to ethanoic anhydride?
(a) SOCl2,Δ
(b) PCl3,Δ
(c) P2O5,Δ
(d) All of these
Answer: c
Question: Diborane easily reduce the functional group such as
(a) acid
(b) ester
(c) nitro
(d) halo
Answer: a
Question: What is the common name of 2-methylpropanoic acid?
(a) Adipic acid
(b) Crotonic acid
(c) Isobutyric acid
(d) Acrylic acid
Answer: c
Question: Aromatic carboxylic acids do not undergo Friedel-Crafts reaction because
(a) carboxyl group acts as an activating and meta-directing group
(b) carboxyl group act as a deactivating and ortho and para directing group
(c) carboxyl group act as an activating and ortho-directing group
(d) carboxyl group acts as deactivating and the catalyst
Answer: b
Question: Which of the following acid is used in rubber, textile, dyeing, leather and electroplating industries?
(a) Hexanedioic acid
(b) Ethanoic acid
(c) Methanoic acid
(d) Sodium benzoate
Answer: c
(i) Rosenmund reduction reaction
(ii) Stephen reaction
(iii) Etard reaction
(iv) Gatterman-Koch reaction
(v) Aldol condensation
(vi) Cross aldol condensation
(vii) Cannizzaro reaction
(viii) Decarboxylation reaction
(ix) Kolbe’s reaction
(x) Hell-Volhard-Zelinsky reaction
(xi) Clemmensen reduction
(xii) Wolff-Kishner reduction
(xii) Haloform reaction.
4. How will you convert :
(i) Isopropyl chloride to 2-methylpropionaldehyde.
(ii) benzene to benzaldehyde
(iii) benzoic acid to acetophenone
(iv) propene to propanal
(v) butanoic acid to 2-hydroxybutanoic acid
(vi) benzoic acid to m-nitrobenzyl alcohol
(vii) propanol to propene
(viii) propanol to butan-2-one.
(ix) methyl magnesium bromide to ethanoic acid
(x) benzoic acid to benzyl chloride
(xi) acetone to chloroform
(xii) acetylene to acetic acid
(xiii) formaldehyde to propanol
(xiv) acetophenone to 2-phenylbutan-2-ol
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CBSE Class 12 Chemistry Unit 12 Aldehydes, Ketones And Carboxylic Acids Assignment
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