All Free Chemistry MCQs with Answers

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13,720 questions · page 548 of 686

  • A. Alkylation of benzene
  • B. Acylation of benzene
  • C. Oxidation of benzene
  • D. Halogenations of benzene
  • E. ABoth A and B

Explanation: Since the acyl group is added to the benzene as a result of this reaction process we can say that it is an acylation of benzene.

Correct answer: Acylation of benzene
  • A. Coloring agent
  • B. Dehydrating agent
  • C. Decolorizing agent
  • D. solubilizing agent

Explanation: Formaldehyde is used in the synthesis of dye fixing agents in dyeing. Also used in disperse dyeing

Correct answer: Decolorizing agent
  • A. Benzaldehyde
  • B. Acetone
  • C. Benzophenone
  • D. Benzyl alcohol

Explanation: OPTION A: Aldehydes that have no a -hydrogen atoms undergo Cannizzaro's reaction.

Correct answer: Benzaldehyde
  • A. Bakelite
  • B. Paraldehyde
  • C. Meta-formaldehyde
  • D. All of these

Explanation: Under acidic conditions, formaldehyde polymerizes to form meta-formaldehyde, which is a cyclic structure comprising 3 formaldehyde…

Correct answer: Meta-formaldehyde
  • A. A
  • B. B
  • C. C
  • D. D

Explanation: Ketone is a functional group with the structure R2C=O, where R can be a variety of carbon-containing substituent

Correct answer: B
  • A. More stearic hindrance offered by its methyl groups
  • B. Electron withdrawing nature of its methyl groups
  • C. Its carbonyl carbon is sp2 hybridized
  • D. Oxygen of carbonyl group is more electronegative than carbon atom

Explanation: Acetone is less reactive towards nucleophilic addition reaction as compared to acetaldehyde due to greater I-effect of the two alkyl group…

Correct answer: More stearic hindrance offered by its methyl groups
  • A. Formaldehyde
  • B. Acetaldehyde
  • C. Dicmthyl ketone
  • D. Propionoldehyde

Explanation: Aldehydes that have no ɑ-hydrogen atoms undergo cannizzaro's reaction. Acetaldehyde possess ɑ-hydrogen therefore it does not give…

Correct answer: Formaldehyde
  • A. They have higher boiling points than that of alkalies
  • B. Theyhave lower boiling points than that of alcohols
  • C. They have higher boiling point than resulting camphor.
  • D. Aldehydes have H-bonding but ketones do not have

Explanation: This statement OPTION D is generally correct. Aldehydes can participate in hydrogen bonding because they have a hydrogen atom directly…

Correct answer: Aldehydes have H-bonding but ketones do not have
  • A. Aldehydes on reduction with NaBH4/H3O+ give 1o alcohol
  • B. Ketones on reduction with NaBH4/H3O+ give 2o alcohol
  • C. Aldehydes on reduction with N2H4/KOH gives alkane
  • D. All of these

Explanation: Option B is correct.No, ketones on reduction with NaBH4/H3O+ do not give 2o alcohols.

Correct answer: Ketones on reduction with NaBH4/H3O+ give 2o alcohol
  • A. Sodium bisulphite
  • B. HCI
  • C. Grignard reagent
  • D. HCN

Explanation: The reason why bulky ketones do not react with sodium bisulphite is because the bulky groups on the ketone make it difficult for the…

Correct answer: Sodium bisulphite
  • A. K2Cr2O7/H2SO4
  • B. HNO3
  • C. Tollen's reagent
  • D. All of these

Explanation: Aldehydes can be oxidized by all of the listed oxidizing agents. Therefore, option d is correct.

Correct answer: All of these
  • A. Sulphide ion
  • B. Sulphite ion
  • C. Hydride ion
  • D. Sodium ion

Explanation: In the addition of sodium bisulfite (NaHSO3) to a carbonyl system, the nucleophile is the sulfite ion (SO32-).

Correct answer: Sulphite ion
  • A. Electrophilic addition
  • B. Electrophilic substitution
  • C. Nucleophilic addition
  • D. Nucleophilic substitution

Explanation: The correct answer is c) Nucleophilic addition. Acetone reacts with HCN through nucleophilic addition to form a cyanohydrin.

Correct answer: Nucleophilic addition
  • A. benzyl alcohol + sodium formate
  • B. sodium benzoate + methanol
  • C. benzyl alcohol + methanol
  • D. sodium benzoate + sodium formate

Explanation: When a mixture of benzaldehyde and formaldehyde is heated with aqueous NaOH (sodium hydroxide) solution, it undergoes a reaction known as…

Correct answer: benzyl alcohol + sodium formate
  • A. sp3 hybridized
  • B. sp hybridized
  • C. sp2 hybridized
  • D. un hybridized

Explanation: In aldehydes and ketones, the carbon of the carbonyl group is indeed sp2 hybridized.

Correct answer: sp2 hybridized
  • A. Formaldehyde
  • B. Acetaldehyde
  • C. Methyl ethyl ketone
  • D. Acetone

Explanation: When calcium acetate undergoes dry distillation, it does indeed result in the formation of acetone.

Correct answer: Acetone
  • A. Butanol
  • B. Propanal
  • C. Propanol
  • D. Butanal

Explanation: In summary, the compound with the highest boiling point among the given options is "a) Butanol." Butanol can form strong hydrogen bonds…

Correct answer: Butanol

10958. The question is

  • A. cyanamide process
  • B. Haber process
  • C. Serpeck's process
  • D. Contact process

Explanation: The Haber process, also called the Haber-Bosch process, is the main industrial procedure for the production of ammonia.

Correct answer: Haber process
  • A. CH3COOH
  • B. HCOOH
  • C. C2H5OH
  • D. Phenol

Explanation: HCOOH, or formic acid, is the strongest acid out of the options

Correct answer: HCOOH
  • A. (CH3)2CO
  • B. C3H7COCH2CH2CH3
  • C. C2H5OC2H5
  • D. C2H5CO(CH2)2CH3

Explanation: The unsymmetrical ketones have two different alkyl groups on either side of carbonyl group like

Correct answer: C2H5CO(CH2)2CH3