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प्रश्न
Convert the following:
Propene to propan-1-ol
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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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संबंधित प्रश्न
Complete the following reaction giving major products.
Name the reagent used to bring about the following conversion.
1-Chloropropane to 1-nitropropane
Give reasons:
Haloarenes are less reactive than haloalkanes.
Convert the following:
Ethanol to propane nitrile
Convert the following:
2-Chloropropane to propan-1-ol
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 it react by SN1 mechanism? Justify your answer.
Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.
Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.
Explain the factors affecting SN1 and SN2 mechanism.
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?
\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]
Compounds X and Y are ____________.
Identify major product 'B' in the following reaction.
\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]
The major product formed when 2-bromobutane is treated with alcoholic KOH is ______.
The compound that reacts the fastest with sodium methoxide is ______.
Explain the dehydrohalogenation reaction of 2-chlorobutane.
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{................}
\end{array}\]
Complete the following reactions giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
Identify the substrate 'X' in the following reaction.
\[\ce{\underset{}{X + O2} ->[i) Co-naphtenate 423 K][ii) dil HClΔ] \underset{\underset{}{}}{Phenol + Acetone}}\]
