Write the structure of the major organic product in each of the following reactions:
CH₃CH₂CH₂Cl + NaI →(acetone) heat
CH₃CH₂CH₂I (1-Iodopropane)
(CH₃)₃CBr + KOH →(ethanol) heat
(CH₃)₂C=CH₂ (2-Methylpropene)
CH₃CH(Br)CH₂CH₃ + NaOH →(water)
CH₃CH(OH)CH₂CH₃ (Butan-2-ol)
CH₃CH₂Br + KCN →(aq. ethanol)
CH₃CH₂CN (Propanenitrile)
C₆H₅ONa + C₂H₅Cl
C₆H₅OC₂H₅ (Ethoxybenzene/Phenetole)
CH₃CH₂CH₂OH + SOCl₂
CH₃CH₂CH₂Cl (1-Chloropropane)
CH₃CH₂CH=CH₂ + HBr →(peroxide)
CH₃CH₂CH₂CH₂Br (1-Bromobutane)
CH₃CH=C(CH₃)₂ + HBr
CH₃CH₂CBr(CH₃)₂ (2-Bromo-2-methylbutane)
Explanation
This question tests nucleophilic substitution and elimination reactions of alkyl halides, along with addition reactions of alkenes. Each sub-part requires identifying the reaction type (SN1, SN2, E1, E2, or electrophilic addition) based on substrate structure, reagent, and solvent conditions.