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Convert the following: tert-Butyl bromide to isobutyl bromide - Chemistry

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प्रश्न

Convert the following:

tert-Butyl bromide to isobutyl bromide

एक पंक्ति में उत्तर

उत्तर

\[\begin{array}{cc}
\ce{\phantom{.........}Br\phantom{.........................................................}H\phantom{............}}\\
\phantom{........}|\phantom{...........................................................}|\phantom{...........}\\
\ce{H3C - C - CH3 +\underset{(Alc.)}{KOH} -> H3C - C = CH2 + HBr ->[Peroxide] H3C - C - CH2Br}\\
\phantom{...}|\phantom{............................}|\phantom{...............................}|\phantom{.....}\\
\ce{\underset{\underset{(2-Bromo-2-methyl propane)}{Tert-Butyl bromide}}{CH3}\phantom{...............}\underset{\underset{(2–Methylprop-1-ene)}{Isobutene}}{CH3}\phantom{....................}\underset{Isobutyl bromide}{CH3}\phantom{...}}\\
\end{array}\]

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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 6. vi. | 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 products.

\[\begin{array}{cc}\ce{CH3 - CH - CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]


Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane


Name the reagent used to bring about the following conversion.

Ethyl bromide to ethyl isocyanide


Name the reagent used to bring about the following conversion.

Chlorobenzene to biphenyl


Distinguish between SN1 and SN2 mechanism of substitution reaction.


Convert the following:

Benzyl alcohol to benzyl cyanide


Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.


Explain the factors affecting SN1 and SN2 mechanism.


Explain aqueous alkaline hydrolysis of tert. butyl bromide.


What is dehydrohalogenation? State the rule for the formation of the preferred product of dehydrohalogenation.


Ethyl bromide undergoes the following reaction:

\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]

Which of the following is a WRONG statement?


Dehydrohalogenation of an alkyl halide is ____________.


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


Which one is most reactive towards nucleophilic addition reaction?


Which of the following is FALSE regarding SN2 reaction mechanism?


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


Convert the following.

p-Nitrochlorobenzene to p-nitrophenol


The compound that reacts the fastest with sodium methoxide is ______.


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Complete the following reaction giving major products.

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


Complete the following reaction giving a major product.

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


Complete the following reaction giving major product.

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


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.

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


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