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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

Complete the following reaction giving major products.

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


Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane


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.

Chlorobenzene to biphenyl


Arrange the following in the increasing order of boiling points.

  1. 1-Bromopropane
  2. 2- Bromopropane
  3. 1- Bromobutane
  4. 1-Bromo-2-methylpropane

Distinguish between SN1 and SN2 mechanism of substitution reaction.


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’.


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.


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


Dehydrohalogenation of an alkyl halide is ____________.


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 of the following carbocation is the most stable?


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


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


With which halogen the reactions, of alkanes are explosive?


Complete the following reaction giving major products.

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


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 react by SN1 mechanism? Justify your answer.


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 reaction giving major product.

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


What is the action of following on ethyl bromide?

alcoholic sodium hydroxide


Complete the reaction:

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


Give a reason for the following:

Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.


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