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प्रश्न
Convert the following:
2-Chloropropane to propan-1-ol
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उत्तर
\[\begin{array}{cc}
\ce{H3C - CH - CH3 ->[Alc.KOH]\underset{Propene}{H3C - CH = CH2}->[HBr][Peroxide]\underset{1-Bromopropane}{H3C - CH2 - CH2Br}->[NaOH(aq.)]\underset{Propan-1-ol}{H3C - CH2 - CH2OH}}\\
|\phantom{...........................................................................................}\\
\ce{\underset{2-Chloropropane}{Cl}\phantom{..........................................................................................}}
\end{array}\]
APPEARS IN
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.
Chlorobenzene to biphenyl
Give reasons:
Haloarenes are less reactive than haloalkanes.
Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.
\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]
Observe the following and answer the question given below.
Comment on the bond length of C–X bond in it.
Propane nitrile can be prepared by heating ____________
The following will react faster by SN1 mechanism
Major product of the following reaction is _______________
\[\ce{CH3-CH2-Mg-Br + NH3 ->?}\]
Explain primary benzylic halide shows higher reactivity by SN1 mechanism than other primary alkyl halide.
Explain the factors affecting SN1 and SN2 mechanism.
Explain aqueous alkaline hydrolysis of tert. butyl bromide.
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?
Identify major product 'B' in the following reaction.
\[\ce{But-1-ene ->[HBr][Peroxide] A ->[AgCN][\Delta] B}\]
What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
Which of the following statements is incorrect regarding the dehydrohalogenation of alkenes?
The order of reactivity of the given haloalkanes towards nucleophiles is:
Explain the dehydrohalogenation reaction of 2-chlorobutane.
Complete the following reaction 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.
Discuss β - elimination reaction.
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:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
Give a reason for the following:
Ethoxy ethane with conc. HI at 373 K gives C2H5OH and CH3I but not CH3OH and C2H5I.
