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महाराष्ट्र राज्य शिक्षण मंडळएचएससी विज्ञान (सामान्य) इयत्ता १२ वी

Major product of the following reaction is _______________ CHX3−CHX2−Mg−Br+NHX3⟶? - Chemistry

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प्रश्न

Major product of the following reaction is _______________

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

पर्याय

  • CH3-CH2-Mg-NH2

  • CH3-CH3

  • Mg-Br-NH2

  • CH3-CH2-Br

MCQ
रिकाम्या जागा भरा

उत्तर

Major product of the following reaction is CH3-CH3

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Chemical Properties
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 10: Halogen Derivatives - Multiple choice questions

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एससीईआरटी महाराष्ट्र Chemistry [English] 12 Standard HSC
पाठ 10 Halogen Derivatives
Multiple choice questions | Q 7

संबंधित प्रश्‍न

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.

1-Chloropropane to 1-nitropropane


Arrange the following in the increasing order of boiling points.

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

Convert the following:

2-Chloropropane to propan-1-ol


Convert the following:

tert-Butyl bromide to isobutyl bromide


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


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 aqueous alkaline hydrolysis of tert. butyl bromide.


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


Which of the following is a primary halide?


Which of the following is least reactive towards SN1 reactions?


\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]

Compounds X and Y are ____________.


Which of the following carbocation is the most stable?


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


What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?


Convert the following.

p-Nitrochlorobenzene to p-nitrophenol


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


With which halogen the reactions, of alkanes are explosive?


Complete the following reaction giving major products.

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


Complete the following reactions giving a major product.

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


Observe the following and answer the question given below:

Can react by SN1 mechanism? Justify your answer.


Discuss β - elimination reaction.


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

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


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 reaction:

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


Identify the chiral molecule from the following.


Complete the following reaction giving major product.

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


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