Methods of Preparation of Ethers
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CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322930 Suitable reaction condition for preparation of methyl phenyl ether is

1 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeOH}\)
2 \(\mathrm{Ph}-\mathrm{Br}, \mathrm{MeO}^{-} \mathrm{Na}^{+}\)
3 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeBr}\)
4 Benzene, MeBr
JEE - 2023
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322931 Which of the following is treated to get anisole?

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{Cl}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{I}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{OH}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322932 The reagent used for the preparation of higher ether from halogenated ethers is

1 Grignard reagent
2 Dry silver oxide
3 Sodium alkoxide
4 conc. \(\mathrm{H}_{2} \mathrm{SO}_{4}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322933 In the reaction,
\(2 \mathrm{~A}+\) dry silver oxide \(\stackrel{\Delta}{\longrightarrow}\) ether \(+2 \mathrm{AgX}\).
A is an/a:

1 Primary alcohol
2 Acid
3 Alkyl halide
4 Alcohol
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322934 \({{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{I + }}\mathop {{\text{A}}{{\text{g}}_{\text{2}}}{\text{O}}}\limits_{{\text{ (Dry) }}} \xrightarrow{\Delta }{\text{Product(A)}}{\text{.}}\) is

1 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OCH}_{3}\)
2 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\)
3 \(\mathrm{C}_{2} \mathrm{H}_{5}-\mathrm{O}-\mathrm{C}_{2} \mathrm{H}_{5}\)
4 \(\mathrm{CH}_{2}=\mathrm{CH}_{2}\)
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CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322930 Suitable reaction condition for preparation of methyl phenyl ether is

1 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeOH}\)
2 \(\mathrm{Ph}-\mathrm{Br}, \mathrm{MeO}^{-} \mathrm{Na}^{+}\)
3 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeBr}\)
4 Benzene, MeBr
JEE - 2023
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322931 Which of the following is treated to get anisole?

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{Cl}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{I}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{OH}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322932 The reagent used for the preparation of higher ether from halogenated ethers is

1 Grignard reagent
2 Dry silver oxide
3 Sodium alkoxide
4 conc. \(\mathrm{H}_{2} \mathrm{SO}_{4}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322933 In the reaction,
\(2 \mathrm{~A}+\) dry silver oxide \(\stackrel{\Delta}{\longrightarrow}\) ether \(+2 \mathrm{AgX}\).
A is an/a:

1 Primary alcohol
2 Acid
3 Alkyl halide
4 Alcohol
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322934 \({{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{I + }}\mathop {{\text{A}}{{\text{g}}_{\text{2}}}{\text{O}}}\limits_{{\text{ (Dry) }}} \xrightarrow{\Delta }{\text{Product(A)}}{\text{.}}\) is

1 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OCH}_{3}\)
2 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\)
3 \(\mathrm{C}_{2} \mathrm{H}_{5}-\mathrm{O}-\mathrm{C}_{2} \mathrm{H}_{5}\)
4 \(\mathrm{CH}_{2}=\mathrm{CH}_{2}\)
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CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322930 Suitable reaction condition for preparation of methyl phenyl ether is

1 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeOH}\)
2 \(\mathrm{Ph}-\mathrm{Br}, \mathrm{MeO}^{-} \mathrm{Na}^{+}\)
3 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeBr}\)
4 Benzene, MeBr
JEE - 2023
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322931 Which of the following is treated to get anisole?

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{Cl}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{I}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{OH}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322932 The reagent used for the preparation of higher ether from halogenated ethers is

1 Grignard reagent
2 Dry silver oxide
3 Sodium alkoxide
4 conc. \(\mathrm{H}_{2} \mathrm{SO}_{4}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322933 In the reaction,
\(2 \mathrm{~A}+\) dry silver oxide \(\stackrel{\Delta}{\longrightarrow}\) ether \(+2 \mathrm{AgX}\).
A is an/a:

1 Primary alcohol
2 Acid
3 Alkyl halide
4 Alcohol
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322934 \({{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{I + }}\mathop {{\text{A}}{{\text{g}}_{\text{2}}}{\text{O}}}\limits_{{\text{ (Dry) }}} \xrightarrow{\Delta }{\text{Product(A)}}{\text{.}}\) is

1 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OCH}_{3}\)
2 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\)
3 \(\mathrm{C}_{2} \mathrm{H}_{5}-\mathrm{O}-\mathrm{C}_{2} \mathrm{H}_{5}\)
4 \(\mathrm{CH}_{2}=\mathrm{CH}_{2}\)
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CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322930 Suitable reaction condition for preparation of methyl phenyl ether is

1 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeOH}\)
2 \(\mathrm{Ph}-\mathrm{Br}, \mathrm{MeO}^{-} \mathrm{Na}^{+}\)
3 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeBr}\)
4 Benzene, MeBr
JEE - 2023
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322931 Which of the following is treated to get anisole?

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{Cl}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{I}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{OH}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322932 The reagent used for the preparation of higher ether from halogenated ethers is

1 Grignard reagent
2 Dry silver oxide
3 Sodium alkoxide
4 conc. \(\mathrm{H}_{2} \mathrm{SO}_{4}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322933 In the reaction,
\(2 \mathrm{~A}+\) dry silver oxide \(\stackrel{\Delta}{\longrightarrow}\) ether \(+2 \mathrm{AgX}\).
A is an/a:

1 Primary alcohol
2 Acid
3 Alkyl halide
4 Alcohol
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322934 \({{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{I + }}\mathop {{\text{A}}{{\text{g}}_{\text{2}}}{\text{O}}}\limits_{{\text{ (Dry) }}} \xrightarrow{\Delta }{\text{Product(A)}}{\text{.}}\) is

1 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OCH}_{3}\)
2 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\)
3 \(\mathrm{C}_{2} \mathrm{H}_{5}-\mathrm{O}-\mathrm{C}_{2} \mathrm{H}_{5}\)
4 \(\mathrm{CH}_{2}=\mathrm{CH}_{2}\)
NEET DIGITAL LIBRARY
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322930 Suitable reaction condition for preparation of methyl phenyl ether is

1 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeOH}\)
2 \(\mathrm{Ph}-\mathrm{Br}, \mathrm{MeO}^{-} \mathrm{Na}^{+}\)
3 \(\mathrm{PhO}^{-} \mathrm{Na}^{+}, \mathrm{MeBr}\)
4 Benzene, MeBr
JEE - 2023
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322931 Which of the following is treated to get anisole?

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{OH}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{Cl}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{ONa}+\mathrm{CH}_{3} \mathrm{I}\)
4 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}+\mathrm{CH}_{3} \mathrm{OH}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322932 The reagent used for the preparation of higher ether from halogenated ethers is

1 Grignard reagent
2 Dry silver oxide
3 Sodium alkoxide
4 conc. \(\mathrm{H}_{2} \mathrm{SO}_{4}\)
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322933 In the reaction,
\(2 \mathrm{~A}+\) dry silver oxide \(\stackrel{\Delta}{\longrightarrow}\) ether \(+2 \mathrm{AgX}\).
A is an/a:

1 Primary alcohol
2 Acid
3 Alkyl halide
4 Alcohol
CHXII11:ALCOHOLS, PHENOLS AND ETHERS

322934 \({{\text{C}}_{\text{2}}}{{\text{H}}_{\text{5}}}{\text{I + }}\mathop {{\text{A}}{{\text{g}}_{\text{2}}}{\text{O}}}\limits_{{\text{ (Dry) }}} \xrightarrow{\Delta }{\text{Product(A)}}{\text{.}}\) is

1 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OCH}_{3}\)
2 \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\)
3 \(\mathrm{C}_{2} \mathrm{H}_{5}-\mathrm{O}-\mathrm{C}_{2} \mathrm{H}_{5}\)
4 \(\mathrm{CH}_{2}=\mathrm{CH}_{2}\)