MCQ
Chloroform can be obtained from
- AMethanol
- BMethanal
- CPropanol $-1$
- ✓Propanol $-2$
✓
Answer
Correct option: D.
Propanol $-2$
d
(d) $CaOC{l_2} + {H_2}O \to Ca{(OH)_2} + C{l_2}$
(d) $CaOC{l_2} + {H_2}O \to Ca{(OH)_2} + C{l_2}$
$\mathop {C{H_3} - \mathop {CH}\limits_{\mathop {|\,\,\,\,}\limits_{OH} } - C{H_3} + C{l_2}}\limits_{{\rm{2 - propanol}}} \to $$C{H_3} - \mathop C\limits_{\mathop {||}\limits_O } - C{H_3} + 2HCl$
$C{H_3} - \mathop {C\,}\limits_{\mathop {||}\limits_O } - C{H_3} + 3C{l_2} \to CC{l_3} - CO - C{H_3} + 3HCl$
Need a full question paper?
Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.
Explore more
Similar questions
Which of the following Fischer projection formula is same as $D-$ Glyceraldehyde ?
→Identify most acidic hydrogen in given compound.
Product obtained in above reactions $(1), (2)$ & $(3)$ is
→The element which forms oxides in all oxidation states $ + I$ to $ + V$ is
→The correct stability order of the following resonance structures of $\mathrm{CH}_3-\mathrm{CH}=\mathrm{CH}-\mathrm{CHO}$ is
→Which of the following molecules will show dipole moment
Product $B$ is
→The alcohol which easily reacts with conc. $HCl $ is
→Which is optically active
Given below are two statements :
→Statement $I :$ The nucleophilic addition of sodium hydrogen sulphite to an aldehyde or a ketone involves proton transfer to form a stable ion.
Statement $II :$ The nucleophilic addition of hydrogen cyanide to an aldehyde or a ketone yields amine as final product.
In the light of the above statements, choose the most appropriate answer from the options given below :