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Free MCQs & Online Quiz Practice for Exams

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    Q: Methanal + CH₃MgBr gives (2016 ETEA)

    A) CH₃CH₂OH
    B) CH₃OH
    C) Manganese
    D) Iodine

    Q: Primary amines on treatment with alkyl halides yield (2016 ETEA)

    A) Secondary amine
    B) Tertiary amine
    C) Quaternary amine
    D) Mixture of a,b,c

    Q: Which is NOT true about Grignard reagent? (2016 ETEA)

    A) Highly reactive
    B) Very stable and easily isolated
    C) Synthetic importance
    D) General formula RMgX

    Q: KOH (alcoholic) + CH(CH₃)₂CH₂Br undergoes (2017 ETEA)

    A) Nucleophilic substitution
    B) Elimination
    C) Nucleophilic addition
    D) None

    Q: OH⁻ (alcoholic) + CH(CH₂)₂Br → product; nature of OH⁻ is (2017 ETEA)

    A) Nucleophile
    B) Lewis base
    C) Ligand
    D) All

    Q: In Wurtz synthesis alkyl halide reacts with sodium; solvent used is (2017 ETEA)

    A) Water
    B) Alcohol
    C) Pyridine
    D) Ether

    Q: In OH⁻ + C₂H₅–I → CH₃CH₂–OH + I⁻, substrate is (2018 ETEA)

    A) OH⁻
    B) CH₃CH₂OH
    C) I⁻
    D) CH₃CH₂I

    Q: Amine most reactive towards HI (2018 ETEA)

    A) Diethyl methyl amine
    B) Dimethyl amine
    C) Methyl propyl amine
    D) Butyl amine

    Q: (CH₃)₃C–CH₂Br cannot undergo elimination with alcoholic KOH because (2018 ETEA)

    A) Alcoholic KOH not good
    B) Tertiary alkyl halide
    C) Strong base needed
    D) No β-hydrogen

    Q: Bromoethane + KCN gives X; reduction of X gives (2018 ETEA)

    A) CH₃CH₃
    B) CH₃CH₂CH₂NH₂
    C) CH₃CH₂COOH
    D) CH₃CH₂CH₂NO₂

    Q: Aqueous KOH causes SN; attacks easiest on (2018 ETEA)

    A) CH₃CH₂Cl
    B) CH₃CH₂Br
    C) CH₃CH₂F
    D) CH₃CH₂I

    Q: 2-bromopropane + C₂H₅S⁻ undergoes (2018 ETEA)

    A) Elimination
    B) Substitution
    C) No reaction
    D) Addition

    Q: Fastest reacting pair (2018 ETEA)

    A) CH₃I + F₂
    B) CH₃Cl + F₂
    C) CH₃Br + Cl₂
    D) CH₃F + I₂

    Q: During SN2 mechanism nucleophile attacks (2019 ETEA)

    A) When C–X bond broken
    B) Before C–X bond broken
    C) When C–H bond broken
    D) After carbocation formation

    Q: Alkyl halides reactive to nucleophile because (2019 ETEA)

    A) Ionic nature
    B) Non-polar C–X bond
    C) Nucleophilic carbon and bad LG
    D) Electrophilic carbon and good LG

    Q: Most soluble in water (2019 ETEA)

    A) Secondary amines
    B) Tertiary amines
    C) Quaternary amines
    D) All insoluble

    Q: Alkyl halide with highest reactivity (2019 ETEA)

    A) R–F
    B) R–Cl
    C) R–Br
    D) R–I

    Q: Stronger nucleophile? (2019 ETEA)

    A) C₂H₅O⁻
    B) C₂H₅S⁻
    C) Both equal
    D) None

    Q: Highest boiling point (2019 ETEA)

    A) Methyl chloride
    B) Methyl iodide
    C) Methyl bromide
    D) Both a and b

    Q: Mechanism where C–X breaks and C–Nu forms simultaneously (2020 ETEA)

    A) SN1
    B) SN2
    C) E1
    D) E2
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