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Complete the following reaction giving major products. CH3−CH(OH) = CH3→[Red P/Br2]→[Ag2O/H2O]B - Chemistry

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प्रश्न

Complete the following reaction giving major products.

\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]

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उत्तर

\[\begin{array}{cc}
\ce{3CH3-CH-CH3->[Red P/Br2][(Bromination)]3CH3-CH-CH3 +H3PO3->[Ag2O/H2O]3CH3-CH-CH3}\\
\phantom{}|\phantom{.............................}|\phantom{.....................................}|\phantom{}\\
\ce{\underset{2-Hydroxypropane}{OH}\phantom{................}\underset{2-Bromopropane(A)}{Br}\phantom{.........................}\underset{Propan-2-ol(B)}{OH}}
\end{array}\]

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Chemical Properties of Halogen Derivatives
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 10: Halogen Derivatives - Exercises [पृष्ठ २३२]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
पाठ 10 Halogen Derivatives
Exercises | Q 2. v. b. | पृष्ठ २३२

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.


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


Convert the following:

Ethanol to propane nitrile


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.

Name the type of halogen derivative.


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 ____________


The following will react faster by SN1 mechanism


Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.


In alkaline hydrolysis of tertiary butyl bromide, ____________.


Which of the following is least reactive towards SN1 reactions?


Which of the following is least reactive towards nucleophilic addition?


Which of the following carbocation is the most stable?


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


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


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


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?


With which halogen the reactions, of alkanes are explosive?


Observe the following and answer the question given below:

Can react by SN1 mechanism? Justify your answer.


Define and explain the SN1 mechanism with a suitable example.


Complete the following reaction giving major product.

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


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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