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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

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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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पाठ 10: Halogen Derivatives - Exercises [पृष्ठ २३३]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
पाठ 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.

1-Chloropropane to 1-nitropropane


Name the reagent used to bring about the following conversion.

Ethyl bromide to ethyl isocyanide


Give reasons:

Haloarenes are less reactive than haloalkanes.


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

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


Observe the following and answer the question given below.

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


Observe the following and answer the question given below.

Can it react by SN1 mechanism? Justify your answer.


Propane nitrile can be prepared by heating ____________


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


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


Explain the factors affecting SN1 and SN2 mechanism.


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


The following mechanism has been proposed for the reaction of NO2 with F2 to form NO2F:

\[\ce{NO2_{(g)} + F2_{(g)} -> NO2F_{(g)} + F_{(g)} (slow)}\]

\[\ce{F_{(g)} + NO2_{(g)} -> NO2F_{(g)} (fast)}\]

The order of the reaction with respect to NO2(g)


How many metameric ethers are represented by the molecular formula C4H10O?


Which one is most reactive towards nucleophilic addition reaction?


What type of hybridisation is present in carbocation formed during the alkaline hydrolysis of 1- bromo-1- phenyl ethane?


Which of the following is FALSE regarding SN2 reaction mechanism?


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


The order of reactivities of the following alkyl halides for an SN2 reaction is ______.


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


Observe the following and answer the questions given below:

Name the type of halogen derivative.


Observe the following and answer the question given below:

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


Define and explain the SN1 mechanism with a suitable example.


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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