English

Name the reagent used to bring about the following conversion. Bromoethane to ethoxyethane - Chemistry

Advertisements
Advertisements

Question

Name the reagent used to bring about the following conversion.

Bromoethane to ethoxyethane

Chart

Solution

Reactant Reagent Product
Bromoethane \[\ce{->[\Delta][sodium alkoxide]}\] Ethoxyethane
shaalaa.com
Chemical Properties
  Is there an error in this question or solution?
Chapter 10: Halogen Derivatives - Exercises [Page 233]

APPEARS IN

Balbharati Chemistry [English] 12 Standard HSC
Chapter 10 Halogen Derivatives
Exercises | Q 2. vi. a. | Page 233

RELATED QUESTIONS

from the following pair would undergo SN2 faster from the other?

a.     b.


from the following pair would undergo SN2 faster from the other?

a. CH3CH2CH2I      b. CH3CH2CH2Cl


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.

\[\begin{array}{cc}\ce{CH3\phantom{................}}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3\phantom{................}}
\end{array}\]


Give reasons:

Haloarenes are less reactive than haloalkanes.


Convert the following:

2-Chloropropane to propan-1-ol


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’.


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.


Explain. Aryl halides are less reactive than alkyl halides towards nucleophilic substitution reactions.


The least reactive towards nucleophilic addition reactions is ____________.


Which of the following is least reactive towards SN1 reactions?


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?


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?


\[\ce{C6H5CH2Cl + KCN(alc) -> X + Y}\]

Compounds X and Y are ____________.


The SN2 reaction of a compound containing an asymmetric carbon atom always gives ____________.


What is the major product obtained in the sulphonation of chlorobenzene with concentrated sulphuric acid?


Which among the following statements is not correct about SN2 reaction mechanism?


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 questions given below:

Name the type of halogen derivative.


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.

\[\begin{array}{cc}
\ce{CH3}\phantom{.................}\\
|\phantom{...................}\\
\ce{CH3 - C - CH2 - Cl ->[Na/dry ether] A}\\
|\phantom{...................}\\
\ce{CH3}\phantom{.................}\\
\end{array}\]


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×