Organic Chemistry Quiz | objective questions | Chemistry General Knowledge Questions | MCQ
- (A) Phosgene
- (B) Chloromethanoyl chloride
- (C) Dichloroketone
- (D) Dichloromethanone
- (A) 5
- (B) 6
- (C) 7
- (D) 8
- (A) Westron
- (B) Perclene
- (C) Westrosol
- (D) Orione
- (A) Polymerization
- (B) Isomerization
- (C) Association
- (D) Dissociation
- (A) Chain isomerism
- (B) Geometrical isomerism
- (C) Metamerism
- (D) Position isomerism
- (A) Metamerism
- (B) Functional isomerism
- (C) Positional isomerism
- (D) All the types
7 >>The least number of carbon atoms for an alkane to show stereoisomerism is: ?
- (A) 2
- (B) 3
- (C) 4
- (D) 5
- (A) Metamerism
- (B) Chain isomerism
- (C) Position isomerism
- (D) Geometrical isomerism
- (A) Oxalic acid
- (B) Benzoic acid
- (C) Acetic acid
- (D) Lactic acid
- (A) Each forms equal number of isomers for a given compound
- (B) If in a compound, one is present, then so is the other
- (C) Both are included in stereoisomerism
- (D) They have no similarity
- (A) 3
- (B) 2
- (C) 4
- (D) 6
- (A) 1,2−dichloro−1−pentene
- (B) 1,3−dichloro−2−pentene
- (C) 1,1−dichloro−1−pentene
- (D) 1,4−dichloro−2−pentene
13 >>Ninhydrin has 3 keto groups. Which keto group is expected to be hydrated more easily? ?
- (A) 2
- (B) 3
- (C) 1
- (D) All equally
- (A) 22.44o
- (B) 90o
- (C) 9.4o
- (D) 0.44o
- (A) RCOOH is more stable than RCOO−
- (B) RCOO− is more stable than RCOOH
- (C) RCOO− and RCOOH do not show resonating structures
- (D) All of the above
- (A) −CN
- (B) −NH2
- (C) −NHR
- (D) −NHCOR
- (A) 9.2, 4.7, 16.0
- (B) 4.8, 9.3, 10.8
- (C) 7.2, 3.7, 3.2
- (D) 2.2, 2.3, 3.8
- (A) 2−butene
- (B) 2−butyne
- (C) 1−butane
- (D) Butane
- (A) H2⁄Ni
- (B) H2⁄Lindlar′s catalyst
- (C) Na⁄liq. NH3
- (D) Zn⁄HCl
- (A) n−butane
- (B) n−pentane
- (C) n−hexane
- (D) n−heptane
- (A) Ethene
- (B) Propene
- (C) cis−2−butene
- (D) trans−2−butene
- (A) m−chlorobenzene
- (B) Benzoyl chloride
- (C) Benzyl chloride
- (D) o− and p−chlorotoluene
- (A) Boat
- (B) Twist boat
- (C) Rigid
- (D) Chair
24 >>Octane number can be changed by: ?
- (A) Isomerization
- (B) Alkylation
- (C) Cyclisation
- (D) All of these
- (A) But−1−yne
- (B) But−2−yne
- (C) But−1−ene
- (D) But−2−ene
- (A) o−xylene
- (B) m−xylene
- (C) p−xylene
- (D) Not possible
- (A) Methane
- (B) Ethane
- (C) Propane
- (D) Butane
- (A) 1−butene
- (B) 2−butene
- (C) Isobutene
- (D) 2−pentene
- (A) Propene
- (B) But−1−ene
- (C) But−2−ene
- (D) Pent−3−ene
- (A) n−heptane
- (B) Cyclohexane
- (C) 3,3−dimethyl pentane
- (D) 2,2,3−trimethyl pentane
- (A) 1,4−diols
- (B) 1,3−diols
- (C) 1,2−diols
- (D) β−ketoaldehyde
- (A) Heating with sodium metal
- (B) Passing dry HCl gas through it
- (C) Distilling it
- (D) Reacting with Mg
- (A) trans−2−methyl cyclohexanol
- (B) cis−2−methyl cycloheaxanol
- (C) 1−methyl cyclohexanol
- (D) Mixture of cis− and trans−2−methyl cyclohexanol
34 >>The function of ZnCl2 in Lucas test for alcohols is: ?
- (A) To act as acid catalyst and react with HCl to form H2ZnCl4
- (B) To act as base catalyst and react with NaOH to form Na2Zn(OH)4
- (C) To act as amphoteric catalyst
- (D) To act as neutral catalyst
- (A) Positive inductive effect of alkyl groups is more than that of hydrogen
- (B) The alkyl group is polar, while hydrogen is not
- (C) Distortion caused by the lone pair of oxygen atom is more than compensated by the bulky alkyl groups
- (D) The hybridisation of oxygen atoms is different in ethers and in water
- (A) C6H5OCH3
- (B) C6H5OC6H5
- (C) C6H5OC3H7
- (D) Tetrahydrofurane
- (A) Meerwein−Ponddorf reaction
- (B) Clemmensen reaction
- (C) Wolff−Kishner reaction
- (D) Schiff reaction
- (A) p−nitrobenzaldehyde
- (B) p−hydroxybenzaldehyde
- (C) Benzaldehyde
- (D) Phenylacetaldehyde
- (A) Benzyl alcohol and sodium formate
- (B) Sodium benzoate and methyl alcohol
- (C) Sodium benzoate and sodium formate
- (D) Benzyl alcohol and methyl alcohol
- (A) Formic acid < Benzoic acid < Acetic acid
- (B) Formic acid < Acetic acid < Benzoic acid
- (C) Acetic acid < Formic acid < Benzoic acid
- (D) Acetic acid < Formic acid < Benzoic acid
- (A) 9 kcal⁄mol
- (B) 19 kcal⁄mol
- (C) 29 kcal⁄mol
- (D) 27 kcal⁄mol
- (A) Equimolar mixture of 1− and 2−butene
- (B) Predominantly 2−butene
- (C) Predominantly 1−butene
- (D) Predominantly 2−butyne
- (A) Ethane
- (B) Ethyne
- (C) Ethene
- (D) Ethane−1,2−diol
- (A) 1
- (B) 2
- (C) 3
- (D) 4
- (A) β−chlorovinyldichloroarsine
- (B) Lewisite
- (C) Nitrobenzene
- (D) Both (1) and (2)
- (A) Ethoxybenzene
- (B) Chlorobenzene
- (C) Ethylbenzoate
- (D) Phenol
- (A) Stereospecific reaction
- (B) Enantiospecific reaction
- (C) Diastereoselective reaction
- (D) Regioselective reaction
- (A) 1−bromo−3−methylbutane
- (B) 2−bromo−3−methylbutane
- (C) 2−bromo−2−methylbutane
- (D) 1−bromo−2−methylbutane
- (A) Mixture of secondary and tertiary alcohols
- (B) Mixture of primary and secondary alcohols
- (C) Secondary or tertiary alcohol
- (D) Primary alcohol
- (A) Subsitution reaction
- (B) Elimination reaction
- (C) Addition reaction
- (D) Rearrangement
- (A) Isobutane
- (B) Isobutylene
- (C) Sodium t−butoxide
- (D) t−butyl methyl ether
- (A) Iso−propyl bromide
- (B) Ethanol
- (C) Ethyl bromide
- (D) None of these
- (A) Cloudiness appears immediately
- (B) Cloudiness appears within 10 minutes
- (C) Cloudiness will not appear at room temperature
- (D) Ketone will be formed in this reaction
- (A) 474 K
- (B) 383 K
- (C) 413 K
- (D) 273 K
- (A) Isobutane < n−butane < n−butyl chloride < n−butanol
- (B) Isobutane < n−butyl chloride < n−butane < n−butanol
- (C) n−butane < n−butanol < n−butyl chloride < isobutane
- (D) n−butane < isobutane < n−butyl chloride < n−butanol
- (A) CO2
- (B) CO
- (C) Oxalic acid
- (D) Acetic acid
- (A) Electrophilic substitution
- (B) Nucleophilic substitution
- (C) Free radical substitution
- (D) Biradical substitution
- (A) Methyl formate
- (B) Isopropyl acetate
- (C) Methyl propionate
- (D) n−propyl formate
- (A) Condensation reaction
- (B) Hydrogen bonding
- (C) Presence of a carboxyl group
- (D) Presence of hydrogen at α−carbon
- (A) 2−hydroxy propanoic acid
- (B) 2−amino propanoic acid
- (C) 2,3−butene−dioic acid
- (D) 2,3−dihydroxy butanoic acid