Q: Methanal + CH₃MgBr gives (2016 ETEA)
Q: Primary amines on treatment with alkyl halides yield (2016 ETEA)
Q: Which is NOT true about Grignard reagent? (2016 ETEA)
Q: KOH (alcoholic) + CH(CH₃)₂CH₂Br undergoes (2017 ETEA)
Q: OH⁻ (alcoholic) + CH(CH₂)₂Br → product; nature of OH⁻ is (2017 ETEA)
Q: In Wurtz synthesis alkyl halide reacts with sodium; solvent used is (2017 ETEA)
Q: In OH⁻ + C₂H₅–I → CH₃CH₂–OH + I⁻, substrate is (2018 ETEA)
Q: Amine most reactive towards HI (2018 ETEA)
Q: (CH₃)₃C–CH₂Br cannot undergo elimination with alcoholic KOH because (2018 ETEA)
Q: Bromoethane + KCN gives X; reduction of X gives (2018 ETEA)
Q: Aqueous KOH causes SN; attacks easiest on (2018 ETEA)
Q: 2-bromopropane + C₂H₅S⁻ undergoes (2018 ETEA)
Q: Fastest reacting pair (2018 ETEA)
Q: During SN2 mechanism nucleophile attacks (2019 ETEA)
Q: Alkyl halides reactive to nucleophile because (2019 ETEA)
Q: Most soluble in water (2019 ETEA)
Q: Alkyl halide with highest reactivity (2019 ETEA)
Q: Stronger nucleophile? (2019 ETEA)
Q: Highest boiling point (2019 ETEA)
Q: Mechanism where C–X breaks and C–Nu forms simultaneously (2020 ETEA)