- A1-butene
- B1-butanol
- C2-butene
- D2-butanol
Explanation:
Alc. KOH is a dehydrohalogenation agent, it reacts with an alkyl halide and alkene forms as a product.
Reaction of process:
$\text{CH}_3\text{CH}_2\text{CH}_2\text{Cl}\xrightarrow{\text{alc.KOH}}\text{CH}_3\text{CH}_2\text{CH}=\text{CH}_2$
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(Given: specific rotations of ($+$)-sucrose, ($+$)-maltose, $L$-($-$)-glucose anc. $+(+)$-fructose in aqueous solution are $+66^{\circ},+140^{\circ},-52^{\circ}$ and $+92^{\circ}$, respectively)
($A$) 'invert sugar' is prepared by acid catalyzed hydrolysis of maltose
($B$) . 'invert sugar' is an equimolar mixture of $D$-($+$)-glucose and $D$-($-$)-fructose
($C$) specific rotation of 'invert sugar' is $-20^{\circ}$
($D$) on reaction with $\mathrm{Br}_2$ water, 'invert sugar' forms saccharic acid as one of the products
