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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.
\[\begin{array}{cc}\ce{CH3 - CH = CH3 ->[Red P/Br2] A ->[Ag2O/H2O]B}\\|\phantom{.........................}\\
\ce{OH\phantom{.......................}}\end{array}\]
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
Arrange the following in the increasing order of boiling points.
- 1-Bromopropane
- 2- Bromopropane
- 1- Bromobutane
- 1-Bromo-2-methylpropane
Complete the following reaction sequence by writing the structural formulae of the organic compound 'A', 'B' and 'C'.
\[\ce{Isopropyl alcohol ->[\triangle][PBr3] A ->[][NH3 excess] B}\]
Propane nitrile can be prepared by heating ____________
The following will react faster by SN1 mechanism
Write the correct order of increasing ease of dehydrohalogenation.
\[\ce{\underset{\text{(I)}}{CH3 - CH2 - CH2 - Cl}}\]
\[\ce{\underset{\text{(II)}}{CH3 - CH(Cl) - CH3}}\]
\[\begin{array}{cc}
\ce{CH3}\\
|\\
\ce{CH3-C-Cl}\phantom{...}\\
|\\
\ce{CH3}\\
\ce{(III)}
\end{array}\]
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 nucleophilic addition?
How many metameric ethers are represented by the molecular formula C4H10O?
Which of the following carbocation is the most stable?
When C2H5Br is treated with excess of alc. NH3, the major product obtained is ____________.
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?
Write the product formed when alkyl halide reacts with silver nitrite.
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 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.
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl->[Na/dry ether]A}\\
|\phantom{..................}\\
\ce{CH3}\phantom{...............}\\
\end{array}\]
What is the action of following on ethyl bromide?
alcoholic sodium hydroxide
Complete the reaction:
\[\ce{CH3CH2Cl ->[AgCN][alc.\Delta]}\] ?
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
