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Name the reagent used to bring about the following conversion. Bromoethane to ethoxyethane - Chemistry

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प्रश्न

Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane

सारिणी

उत्तर

Reactant Reagent Product
Bromoethane \[\ce{->[\Delta][sodium alkoxide]}\] Ethoxyethane
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Chemical Properties
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अध्याय 10: Halogen Derivatives - Exercises [पृष्ठ २३३]

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बालभारती Chemistry [English] 12 Standard HSC
अध्याय 10 Halogen Derivatives
Exercises | Q 2. vi. a. | पृष्ठ २३३

संबंधित प्रश्न

Complete the following reaction giving major products.

\[\ce{CH3 - CH = CH2 ->[HBr][peroxide] A ->[alc. KOH] B}\]


Complete the following reaction giving major product.

\[\begin{array}{cc}\ce{CH3\phantom{................}}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3\phantom{................}}
\end{array}\]


Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

2-Chloropropane to propan-1-ol


Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.

\[\ce{2-Bromobutane->[Alc.KOH]A->[][Br2]B->[][NaNH2]C}\]


Nucleophilic substitution reaction of 2, 4-dinitrochlorobenzene is faster than p-nitrochlorobenzene. Give reason.


Write the correct order of increasing ease of dehydrohalogenation.

\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]

\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]

\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]


Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.


Explain aqueous alkaline hydrolysis of tert. butyl bromide.


Which of the following is least reactive towards nucleophilic addition?


Nitroalkanes are obtained in laboratory from primary or secondary alkyl halides by the action of ______.


\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]

Compounds X and Y are ____________.


Which of the following carbocation is the most stable?


Which of the following is FALSE regarding SN2 reaction mechanism?


The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.


Identify 'B' in the following reaction.

\[\ce{2-Bromobutane ->[KOH alc.][\Delta] A ->[HI] B}\]


Write the product formed when alkyl halide reacts with silver nitrite.


With which halogen the reactions, of alkanes are explosive?


Explain the dehydrohalogenation reaction of 2-chlorobutane.


Complete the following reaction giving a major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]


Observe the following and answer the question given below:

Comment on the bond length of C-X bond in it.


Complete the following reaction sequences by writing the structural formulae of the organic compounds 'A', 'B' and 'C'.

\[\ce{2-Bromobutan ->[alc. KOH] A ->[][Br2] B ->[][NANH2] C}\]


Complete the following reactions giving major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]


Complete the reaction:

\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?


Identify the chiral molecule from the following.


Complete the following reaction giving major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]


Complete the following reaction giving major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]


Complete the following reaction giving major product.

\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]


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