Advertisements
Advertisements
प्रश्न
Name the reagent used to bring about the following conversion.
Bromoethane to ethoxyethane
Advertisements
उत्तर
| Reactant | Reagent | Product |
| Bromoethane | \[\ce{->[\Delta][sodium alkoxide]}\] | Ethoxyethane |
APPEARS IN
संबंधित प्रश्न
from the following pair would undergo SN2 faster from the other?
a. CH3CH2CH2I b. CH3CH2CH2Cl
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.
1-Chloropropane to 1-nitropropane
Convert the following:
Benzyl alcohol to benzyl cyanide
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.
Name the type of halogen derivative.
Observe the following and answer the question given below.
Can it react by SN1 mechanism? Justify your answer.
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 a primary halide?
Ethyl bromide undergoes the following reaction:
\[\ce{\underset{Ethyl bromide}{C2H5Br} + \underset{(aq.)}{KOH} ->[\Delta] \underset{Ethyl alcohol}{C2H5OH} + KBr}\]
Which of the following is a WRONG statement?
Which of the following is least reactive towards nucleophilic addition?
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?
When C2H5Br is treated with excess of alc. NH3, the major product obtained is ____________.
Identify 'B' in the following reaction.
\[\ce{2-Bromobutane ->[KOH alc.][\Delta] A ->[HI] B}\]
The order of reactivities of the following alkyl halides for an SN2 reaction is ______.
The order of reactivity of the given haloalkanes towards nucleophiles is:
With which halogen the reactions, of alkanes are explosive?
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:
Can react by SN1 mechanism? Justify your answer.
Complete the following reaction giving major product.
\[\begin{array}{cc}
\ce{CH3}\phantom{...............}\\
|\phantom{..................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}
\end{array}\]
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.
\[\begin{array}{cc}
\ce{CH3}\phantom{................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl->[Na/ dry ether]A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{................}\\
\end{array}\]
