Question
Complete the following reaction:$\text{C}_6\text{H}_5\text{N}_2\text{Cl}+\text{C}_2\text{H}_5\text{OH}\rightarrow$
✓
Answer
$ \ \ \ \ \ \ \ \ \ \ \ \ \text{C}_6\text{H}_5\text{N}_2\text{Cl} \ \ + \ \ \ \text{C}_2\text{H}_5\text{OH}\rightarrow\text{C}_6\text{H}_6+\text{CH}_3\text{CHO}+\text{N}_2+\text{HCl}\\\text{Benzenediazonium} \ \ \ \ \ \ \ \text{Ethanol} \ \ \ \ \ \ \ \text{Benzene} \ \ \ \ \ \text{Ethanal}\\ \ \ \ \ \ \ \ \ \ \ \ \text{Cloride}$
Need a full question paper?
Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.
Explore more
Similar questions
Write the structures of the following organic halogen compound. 4-tert-Butyl-3-iodoheptane.
Give an example of a substance that can act as a disinfectant as well as antiseptic depending upon its concentration. (Specify concentration)
Write the IUPAC name of the given compound.
Pickles have a long shelf life and do not get spoiled for months, why?
Give the IUPAC name of the following compound: $\mathrm{Ph} \mathrm{~CH}_2 \mathrm{CH}_2 \mathrm{COOH}$.
→Explain Swartz reaction by an example.
Read the given passage and answer the questions number 1 to 5 that follow:
The substitution reaction of alkyl halide mainly occurs by $S_N1$ or $S_N2$ mechanism. Whatever mechanism alkyl halides follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution reactions. The rate of $S_N1$ reactions are governed by the stability of carbocation whereas for $S_N2$ reactions steric factor is the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with HI is also governed by steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in deciding the kind of product formed.
Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes substitution reaction by $S_N1$ mechanism.
→The substitution reaction of alkyl halide mainly occurs by $S_N1$ or $S_N2$ mechanism. Whatever mechanism alkyl halides follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution reactions. The rate of $S_N1$ reactions are governed by the stability of carbocation whereas for $S_N2$ reactions steric factor is the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with HI is also governed by steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in deciding the kind of product formed.
Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes substitution reaction by $S_N1$ mechanism.
What are secondary cells?
Write the equations for the preparation of 1-iodobutane from:
but-1-ene.
but-1-ene.
What is aspartame and what is its use?