322948
The major product of the reaction between ter-butyl chloride and sodium ethoxide is:
1 2-Methyl prop - 1 - ene
2 1 - Butene
3 2 - Butene
4 Ethene
Explanation:
Tertiary alkyl halides undergo elimination when treated with strong bases like sodium ethoxide.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322949
In the Williamson synthesis of ethers given by the general equation \(\mathrm{R}-\mathrm{X}+\mathrm{R}^{1} \mathrm{ONa} \longrightarrow \mathrm{R}-\mathrm{O}-\mathrm{R}^{1}\). The yield form \(\mathrm{R}-\mathrm{X}\) follows the sequence
1 \(\mathrm{CH}_{3}>1^{0}>2^{0}>3^{0}\)
2 \(\mathrm{CH}_{3} < 1^{0} < 2^{0} < 3^{0}\)
3 \(\mathrm{CH}_{3} < 1^{0}>2^{0}>3^{0}\)
4 \(\mathrm{CH}_{3}>1^{0} < 2^{0} < 3^{0}\)
Explanation:
\(3^\circ \,\,{\text{RX}}\) produces alkene with \(\mathrm{R}^{1} \mathrm{ONa}\) instead of ethers.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322950
The reaction can be classified as:
1 Alcohol formation reaction
2 Dehydration reaction
3 Williamson alcohol synthesis reaction
4 Williamson ether synthesis reaction
Explanation:
This is williamson ether synthesis.
NEET - 2016
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322951
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{ONa}}}}{\text{Ethoxyethane}}{\text{.}}\) ' A ' and ' B ' are respectively
322948
The major product of the reaction between ter-butyl chloride and sodium ethoxide is:
1 2-Methyl prop - 1 - ene
2 1 - Butene
3 2 - Butene
4 Ethene
Explanation:
Tertiary alkyl halides undergo elimination when treated with strong bases like sodium ethoxide.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322949
In the Williamson synthesis of ethers given by the general equation \(\mathrm{R}-\mathrm{X}+\mathrm{R}^{1} \mathrm{ONa} \longrightarrow \mathrm{R}-\mathrm{O}-\mathrm{R}^{1}\). The yield form \(\mathrm{R}-\mathrm{X}\) follows the sequence
1 \(\mathrm{CH}_{3}>1^{0}>2^{0}>3^{0}\)
2 \(\mathrm{CH}_{3} < 1^{0} < 2^{0} < 3^{0}\)
3 \(\mathrm{CH}_{3} < 1^{0}>2^{0}>3^{0}\)
4 \(\mathrm{CH}_{3}>1^{0} < 2^{0} < 3^{0}\)
Explanation:
\(3^\circ \,\,{\text{RX}}\) produces alkene with \(\mathrm{R}^{1} \mathrm{ONa}\) instead of ethers.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322950
The reaction can be classified as:
1 Alcohol formation reaction
2 Dehydration reaction
3 Williamson alcohol synthesis reaction
4 Williamson ether synthesis reaction
Explanation:
This is williamson ether synthesis.
NEET - 2016
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322951
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{ONa}}}}{\text{Ethoxyethane}}{\text{.}}\) ' A ' and ' B ' are respectively
322948
The major product of the reaction between ter-butyl chloride and sodium ethoxide is:
1 2-Methyl prop - 1 - ene
2 1 - Butene
3 2 - Butene
4 Ethene
Explanation:
Tertiary alkyl halides undergo elimination when treated with strong bases like sodium ethoxide.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322949
In the Williamson synthesis of ethers given by the general equation \(\mathrm{R}-\mathrm{X}+\mathrm{R}^{1} \mathrm{ONa} \longrightarrow \mathrm{R}-\mathrm{O}-\mathrm{R}^{1}\). The yield form \(\mathrm{R}-\mathrm{X}\) follows the sequence
1 \(\mathrm{CH}_{3}>1^{0}>2^{0}>3^{0}\)
2 \(\mathrm{CH}_{3} < 1^{0} < 2^{0} < 3^{0}\)
3 \(\mathrm{CH}_{3} < 1^{0}>2^{0}>3^{0}\)
4 \(\mathrm{CH}_{3}>1^{0} < 2^{0} < 3^{0}\)
Explanation:
\(3^\circ \,\,{\text{RX}}\) produces alkene with \(\mathrm{R}^{1} \mathrm{ONa}\) instead of ethers.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322950
The reaction can be classified as:
1 Alcohol formation reaction
2 Dehydration reaction
3 Williamson alcohol synthesis reaction
4 Williamson ether synthesis reaction
Explanation:
This is williamson ether synthesis.
NEET - 2016
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322951
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{ONa}}}}{\text{Ethoxyethane}}{\text{.}}\) ' A ' and ' B ' are respectively
322948
The major product of the reaction between ter-butyl chloride and sodium ethoxide is:
1 2-Methyl prop - 1 - ene
2 1 - Butene
3 2 - Butene
4 Ethene
Explanation:
Tertiary alkyl halides undergo elimination when treated with strong bases like sodium ethoxide.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322949
In the Williamson synthesis of ethers given by the general equation \(\mathrm{R}-\mathrm{X}+\mathrm{R}^{1} \mathrm{ONa} \longrightarrow \mathrm{R}-\mathrm{O}-\mathrm{R}^{1}\). The yield form \(\mathrm{R}-\mathrm{X}\) follows the sequence
1 \(\mathrm{CH}_{3}>1^{0}>2^{0}>3^{0}\)
2 \(\mathrm{CH}_{3} < 1^{0} < 2^{0} < 3^{0}\)
3 \(\mathrm{CH}_{3} < 1^{0}>2^{0}>3^{0}\)
4 \(\mathrm{CH}_{3}>1^{0} < 2^{0} < 3^{0}\)
Explanation:
\(3^\circ \,\,{\text{RX}}\) produces alkene with \(\mathrm{R}^{1} \mathrm{ONa}\) instead of ethers.
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322950
The reaction can be classified as:
1 Alcohol formation reaction
2 Dehydration reaction
3 Williamson alcohol synthesis reaction
4 Williamson ether synthesis reaction
Explanation:
This is williamson ether synthesis.
NEET - 2016
CHXII11:ALCOHOLS, PHENOLS AND ETHERS
322951
\({\text{A}}\xrightarrow{{{\text{HBr}}}}{\text{B}}\xrightarrow{{{{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{ONa}}}}{\text{Ethoxyethane}}{\text{.}}\) ' A ' and ' B ' are respectively
