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 these10952. In the addition of sodium bisulfite to carbonyl system, which of the following is nucleophile?
- 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: Butanol10958. 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