हिंदी

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'.

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

एक पंक्ति में 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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अध्याय 10: Halogen Derivatives - Exercises [पृष्ठ २३३]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
अध्याय 10 Halogen Derivatives
Exercises | Q 7. ii. b. | पृष्ठ २३३

संबंधित प्रश्न

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

a. CH3CH2CH2I      b. CH3CH2CH2Cl


Complete the following reaction giving major products.

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


Complete the following reaction giving major product.

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


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


Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

Ethanol to propane nitrile


Convert the following:

2-Chloropropane to propan-1-ol


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.


In alkaline hydrolysis of tertiary butyl bromide, ____________.


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


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)


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 carbocation is the most stable?


When C2H5Br is treated with excess of alc. NH3, the major product obtained is ____________.


Identify 'B' in the following reaction.

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


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


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


Explain the dehydrohalogenation reaction of 2-chlorobutane.


Complete the following reaction giving a major product.

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


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

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


Identify the chiral molecule from the following.


Complete the following reaction giving major product.

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


Which among the following is NOT benzylic halide?


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