The order of reactivity of alcohols with a given haloacid (HCl, HBr, HI) is:
AAllylic = Benzylic only
BPrimary > Secondary > Tertiary
CTertiary > Secondary > Primary (3° > 2° > 1°)
DPrimary = Secondary = Tertiary
Answer & Solution
Correct answer: C. Tertiary > Secondary > Primary (3° > 2° > 1°)
Reactivity with HX follows **3° > 2° > 1°**.
Mechanism is SN1 — proceeds via a **carbocation**, and tertiary carbocations are most stable.
Primary alcohols + HCl need **ZnCl₂ catalyst** (Lucas reagent)
tertiary alcohols react at room temp without catalyst.
Keep practising Haloalkanes and Haloarenes
Browse all Haloalkanes and Haloarenes questions for AP Intermediate 2nd Year, or explore more Chemistry topics.
Related questions
As per your syllabus, the STAGGERED form of ethane is more stable than ECLIPSED for which As per your syllabus, Mechanism, the FIRST step of methane chlorination under sunlight is As per your syllabus, the rate of substitution of HYDROGENS in alkane halogenation goes inAs per your syllabus, the rate of HALOGENATION of alkanes (F₂, Cl₂, Br₂, I₂) decreases in As per your syllabus, (ii), in Kolbe electrolytic synthesis of alkanes, the alkane gas is As per your syllabus, (i), heating CH₃COONa with NaOH + CaO (soda-lime) produces which gasAs per your syllabus, (ii), the Wurtz reaction uses which reagent + solvent for coupling aAs per your syllabus, + Fig 9.1, the H-C-H bond angle in methane and the carbon hybridisat