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Question: In the below reaction, the reactivity of alcohols is; \(ROH + HX \to RX + {H_2}O\) ; A) \[Terti...

In the below reaction, the reactivity of alcohols is;
ROH+HXRX+H2OROH + HX \to RX + {H_2}O ;
A) Tertiary > secondary > primaryTertiary{\text{ }} > {\text{ }}secondary{\text{ }} > {\text{ }}primary
B) Tertiary < secondary < primaryTertiary{\text{ }} < {\text{ }}secondary{\text{ }} < {\text{ }}primary
C) Tertiary > primary > secondaryTertiary{\text{ }} > {\text{ }}primary{\text{ }} > {\text{ }}secondary
D) Secondary > primary > tertiarySecondary{\text{ }} > {\text{ }}primary{\text{ }} > {\text{ }}tertiary

Explanation

Solution

Alcohols are compounds in which a hydroxyl (– OH) group is attached to saturated carbon atom.
General Formula: ROHR - OH
Monohydric alcohols are classified as primary (1°) secondary (2°), or tertiary (3°), depending upon whether the –OH group is attached to a primary, a secondary, or a tertiary carbon.

Complete step by step answer: Alcohols are reactive compounds. They are attacked by polar or ionic reagents. This is because:
The C–O and O–H bonds of the alcohols are polar since oxygen is highly electronegative.

They oxygen atoms of alcohols is an electron-rich centre because it has two unshared pairs of electrons
Alcohols react with hydrogen (HXHX) to form the corresponding alkyl halides
Eg; CH3CH2OH+HBrCH3CH2Br+H2OC{H_3}C{H_2}OH + HBr \to C{H_3}C{H_2}Br + {H_2}O
In general, tertiary alcohols react rapidly with hydrogen halides; secondary alcohols react somewhat slower; and primary alcohols, even more slowly.
The reaction is acid catalyzed. Alcohols react with the strongly acidic hydrogen halides HCl, HBrHCl,{\text{ }}HBr , and {\text{ }}HI], but they do not react with non acidic NaCl, NaBr, or NaINaCl,{\text{ }}NaBr,{\text{ }}or{\text{ }}NaI . Primary and secondary alcohols can be converted to alkyl chlorides and bromides by allowing them to react with a mixture of a sodium halide and sulfuric acid:
The order of reactivity of alcohols is 3>2>13^\circ > 2^\circ > 1^\circ methyl.

So,Option “A” is correct.
Note: The order of reactivity of hydrogen halidesis HI > HBr > HClis{\text{ }}HI{\text{ }} > {\text{ }}HBr{\text{ }} > {\text{ }}HCl . HClHCl reacts only in the presence of a catalyst anhydrous(ZnCl2)(ZnC{l_2}) .No catalyst is required in the case of HBr or HIHBr{\text{ }}or{\text{ }}HI.
Primary alcohols react with hydrogen halides by an SN1{S_N}1 mechanism.