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Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'. Isopropyl alcohol→PBrX3△A→NHX3 excessB

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प्रश्न

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

\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]

एका वाक्यात उत्तर
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उत्तर

\[\begin{array}{cc}
\ce{H3C - CH - OH ->[\triangle][PBr3] H3C - CH - Br ->[NH3, Excess]H3C - CH - NH2}\\
|\phantom{......................}|\phantom{..........................}|\phantom{..}\\
\phantom{.......}\ce{\underset{\text{Isopropyl alcohol}}{CH3}\phantom{.......}}
\ce{\underset{\text{Isopropyl bromide (A)}}{CH3}\phantom{.........}\phantom{}}
\ce{\underset{\text{Propan-2-amine (B)}}{CH3}}
\end{array}\]

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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 7. ii. b. | पृष्ठ २३३

संबंधित प्रश्‍न

from the following pair would undergo SN2 faster from the other?

  1.    

Complete the following reaction giving major products.


Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane


Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

Propene to propan-1-ol


Convert the following:

Ethanol to propane nitrile


Convert the following:

2-Chloropropane to propan-1-ol


Convert the following:

tert-Butyl bromide to isobutyl bromide


HCl is added to a hydrocarbon ‘A’ \[\ce{(C4H8)}\] to give a compound ‘B’ which on hydrolysis with aqueous alkali forms tertiary alcohol ‘C’ \[\ce{(C4H10O)}\]. Identify ‘A’ ,‘B’ and ‘C’.


Observe the following and answer the question given below.

Can it react by SN1 mechanism? Justify your answer.


The following will react faster by SN1 mechanism


Major product of the following reaction is _______________

\[\ce{CH3-CH2-Mg-Br + NH3 ->?}\]


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 the factors affecting SN1 and SN2 mechanism.


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


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


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


Identify major product 'B' in the following reaction.

\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]


The major product formed when 2-bromobutane is treated with alcoholic KOH is ______.


Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?


Which among the following statements is not correct about SN2 reaction mechanism?


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.


Complete the following reactions giving major product.

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


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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