How will you convert:
$(i)$ Ethanoic acid into methanamine
$(ii)$ Hexanenitrile into $1$-aminopentane
$(iii)$ Methanol to ethanoic acid
$(iv)$ Ethanamine into methanamine
$(v)$ Ethanoic acid into propanoic acid
$(vi)$ Methanamine into ethanamine
$(vii)$ Nitromethane into dimethylamine
$(viii)$ Propanoic acid into ethanoic acid?
$(i)$ Ethanoic acid into methanamine
$(ii)$ Hexanenitrile into $1$-aminopentane
$(iii)$ Methanol to ethanoic acid
$(iv)$ Ethanamine into methanamine
$(v)$ Ethanoic acid into propanoic acid
$(vi)$ Methanamine into ethanamine
$(vii)$ Nitromethane into dimethylamine
$(viii)$ Propanoic acid into ethanoic acid?
(N/A) $(i)$ $\text{CH}_3\text{COOH}$ $\xrightarrow{\text{SOCl}_2} \text{CH}_3\text{COCl}$ $\xrightarrow{\text{NH}_3} \text{CH}_3\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{NaOH}} \text{CH}_3\text{NH}_2$
$(ii)$ $\text{C}_5\text{H}_{11}\text{CN}$ $\xrightarrow{\text{H}^+/\text{H}_2\text{O}} \text{C}_5\text{H}_{11}\text{COOH}$ $\xrightarrow{\text{SOCl}_2} \text{C}_5\text{H}_{11}\text{COCl}$ $\xrightarrow{\text{NH}_3} \text{C}_5\text{H}_{11}\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{KOH}} \text{C}_5\text{H}_{11}\text{NH}_2$
$(iii)$ $\text{CH}_3\text{OH}$ $\xrightarrow{\text{PCl}_5} \text{CH}_3\text{Cl}$ $\xrightarrow{\text{KCN}} \text{CH}_3\text{CN}$ $\xrightarrow{\text{H}^+/\text{H}_2\text{O}} \text{CH}_3\text{COOH}$
$(iv)$ $\text{CH}_3\text{CH}_2\text{NH}_2$ $\xrightarrow{\text{NaNO}_2/\text{HCl}} \text{CH}_3\text{CH}_2\text{OH}$ $\xrightarrow{\text{KMnO}_4} \text{CH}_3\text{COOH}$ $\xrightarrow{\text{NH}_3, \Delta} \text{CH}_3\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{NaOH}} \text{CH}_3\text{NH}_2$
$(v)$ $\text{CH}_3\text{COOH}$ $\xrightarrow{\text{LiAlH}_4} \text{CH}_3\text{CH}_2\text{OH}$ $\xrightarrow{\text{PCl}_5} \text{CH}_3\text{CH}_2\text{Cl}$ $\xrightarrow{\text{KCN}} \text{CH}_3\text{CH}_2\text{CN}$ $\xrightarrow{\text{H}^+/\text{H}_2\text{O}} \text{CH}_3\text{CH}_2\text{COOH}$
$(vi)$ $\text{CH}_3\text{NH}_2$ $\xrightarrow{\text{NaNO}_2/\text{HCl}} \text{CH}_3\text{OH}$ $\xrightarrow{\text{PCl}_5} \text{CH}_3\text{Cl}$ $\xrightarrow{\text{KCN}} \text{CH}_3\text{CN}$ $\xrightarrow{\text{H}_2/\text{Ni}} \text{CH}_3\text{CH}_2\text{NH}_2$
$(vii)$ $\text{CH}_3\text{NO}_2$ $\xrightarrow{\text{Sn/HCl}} \text{CH}_3\text{NH}_2$ $\xrightarrow{\text{CHCl}_3/\text{KOH}} \text{CH}_3\text{NC}$ $\xrightarrow{\text{Na/C}_2\text{H}_5\text{OH}} \text{CH}_3\text{NHCH}_3$
$(viii)$ $\text{CH}_3\text{CH}_2\text{COOH}$ $\xrightarrow{\text{NH}_3, \Delta} \text{CH}_3\text{CH}_2\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{KOH}} \text{CH}_3\text{CH}_2\text{NH}_2$ $\xrightarrow{\text{NaNO}_2/\text{HCl}} \text{CH}_3\text{CH}_2\text{OH}$ $\xrightarrow{\text{KMnO}_4} \text{CH}_3\text{COOH}$
$(ii)$ $\text{C}_5\text{H}_{11}\text{CN}$ $\xrightarrow{\text{H}^+/\text{H}_2\text{O}} \text{C}_5\text{H}_{11}\text{COOH}$ $\xrightarrow{\text{SOCl}_2} \text{C}_5\text{H}_{11}\text{COCl}$ $\xrightarrow{\text{NH}_3} \text{C}_5\text{H}_{11}\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{KOH}} \text{C}_5\text{H}_{11}\text{NH}_2$
$(iii)$ $\text{CH}_3\text{OH}$ $\xrightarrow{\text{PCl}_5} \text{CH}_3\text{Cl}$ $\xrightarrow{\text{KCN}} \text{CH}_3\text{CN}$ $\xrightarrow{\text{H}^+/\text{H}_2\text{O}} \text{CH}_3\text{COOH}$
$(iv)$ $\text{CH}_3\text{CH}_2\text{NH}_2$ $\xrightarrow{\text{NaNO}_2/\text{HCl}} \text{CH}_3\text{CH}_2\text{OH}$ $\xrightarrow{\text{KMnO}_4} \text{CH}_3\text{COOH}$ $\xrightarrow{\text{NH}_3, \Delta} \text{CH}_3\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{NaOH}} \text{CH}_3\text{NH}_2$
$(v)$ $\text{CH}_3\text{COOH}$ $\xrightarrow{\text{LiAlH}_4} \text{CH}_3\text{CH}_2\text{OH}$ $\xrightarrow{\text{PCl}_5} \text{CH}_3\text{CH}_2\text{Cl}$ $\xrightarrow{\text{KCN}} \text{CH}_3\text{CH}_2\text{CN}$ $\xrightarrow{\text{H}^+/\text{H}_2\text{O}} \text{CH}_3\text{CH}_2\text{COOH}$
$(vi)$ $\text{CH}_3\text{NH}_2$ $\xrightarrow{\text{NaNO}_2/\text{HCl}} \text{CH}_3\text{OH}$ $\xrightarrow{\text{PCl}_5} \text{CH}_3\text{Cl}$ $\xrightarrow{\text{KCN}} \text{CH}_3\text{CN}$ $\xrightarrow{\text{H}_2/\text{Ni}} \text{CH}_3\text{CH}_2\text{NH}_2$
$(vii)$ $\text{CH}_3\text{NO}_2$ $\xrightarrow{\text{Sn/HCl}} \text{CH}_3\text{NH}_2$ $\xrightarrow{\text{CHCl}_3/\text{KOH}} \text{CH}_3\text{NC}$ $\xrightarrow{\text{Na/C}_2\text{H}_5\text{OH}} \text{CH}_3\text{NHCH}_3$
$(viii)$ $\text{CH}_3\text{CH}_2\text{COOH}$ $\xrightarrow{\text{NH}_3, \Delta} \text{CH}_3\text{CH}_2\text{CONH}_2$ $\xrightarrow{\text{Br}_2/\text{KOH}} \text{CH}_3\text{CH}_2\text{NH}_2$ $\xrightarrow{\text{NaNO}_2/\text{HCl}} \text{CH}_3\text{CH}_2\text{OH}$ $\xrightarrow{\text{KMnO}_4} \text{CH}_3\text{COOH}$
Explore More
Similar Questions
An organic compound $A$ contains nitrogen and chlorine. It dissolves readily in water to give a solution that turns litmus red. Titration of compound $A$ with standard base indicates that the molecular weight of $A$ is $131 \pm 2$. When a sample of $A$ is treated with aqueous $NaOH$,a liquid separates which contains $N$ but not $Cl$. Treatment of the obtained liquid with nitrous acid followed by phenol gives an orange precipitate. The compound $A$ is:
DifficultJEE MAIN 2022
View SolutionWhich of the following statements is not true?
MediumAIIMS 2011
View SolutionIn the given reaction,$A$ is:
$A$ $\xrightarrow{\text{Reduction}} B$ $\xrightarrow{HNO_2} C_2H_5OH$
$A$ $\xrightarrow{\text{Reduction}} B$ $\xrightarrow{HNO_2} C_2H_5OH$
Difficult
View SolutionWhen you ingest aspirin,it passes through your stomach,which has an acidic $pH$,before traveling through the basic environment of your intestine. Provide the structure form as it exists in the intestine.
Difficult
View SolutionWrite $IUPAC$ names of the following compounds and classify them into primary,secondary,and tertiary amines.
$(i)$ $(CH_3)_2CHNH_2$
$(ii)$ $CH_3(CH_2)_2NH_2$
$(iii)$ $CH_3NHCH(CH_3)_2$
$(iv)$ $(CH_3)_3CNH_2$
$(v)$ $C_6H_5NHCH_3$
$(vi)$ $(CH_3CH_2)_2NCH_3$
$(vii)$ $m-BrC_6H_4NH_2$
$(i)$ $(CH_3)_2CHNH_2$
$(ii)$ $CH_3(CH_2)_2NH_2$
$(iii)$ $CH_3NHCH(CH_3)_2$
$(iv)$ $(CH_3)_3CNH_2$
$(v)$ $C_6H_5NHCH_3$
$(vi)$ $(CH_3CH_2)_2NCH_3$
$(vii)$ $m-BrC_6H_4NH_2$
Medium
View SolutionVedclass Products
For Students
Vedclass Test Series
Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.
Start Free TrialFor Teachers
Exam Paper Generator
Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.
Try FreeFor Institutes
Online Exam Module
Live online exams with unlimited students, 360° analytics & white-label branding.
See Demo