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Convert the following: Propene to propan-1-ol - Chemistry

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प्रश्न

Convert the following:

Propene to propan-1-ol

एका वाक्यात उत्तर
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उत्तर

\[\ce{\underset{\text{Propene}}{H3C - CH = CH2 + HBr} ->[Peroxide] \underset{\text{1-Bromopropane}}{H3C - CH2 - CH2Br} + \underset{\text{(aq.)}}{NaOH} ->[\triangle]\underset{\text{Propan-1-ol}}{CH3CH2CH2OH} + NaBr}\]

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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 6. i. | पृष्ठ २३३

संबंधित प्रश्‍न

Complete the following reaction giving major products.

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


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.

Chlorobenzene to biphenyl


Convert the following:

Benzyl alcohol to benzyl cyanide


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’.


Propane nitrile can be prepared by heating ____________


The following will react faster by SN1 mechanism


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.


Explain the factors affecting SN1 and SN2 mechanism.


Explain aqueous alkaline hydrolysis of tert. butyl bromide.


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


The least reactive towards nucleophilic addition reactions is ____________.


Which of the following is least reactive towards SN1 reactions?


Which of the following is FALSE regarding SN2 reaction mechanism?


Identify major product 'B' in the following reaction.

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


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


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:

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 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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