Answer:
We can do the nitration of benzene by treating the benzene with a mixture of nitric acid and sulphuric acid by not extending the temperature of 50°C
Explanation:
Nitration of benzene takes place by treating the benzene with a mixture of nitric acid and sulphuric acid at low temperatures such as the temperatures below 50°C
The nitration of benzene takes place through electrophilic substitution reaction
In this reaction the electrophile is nitronium ion (NO2+) which performs an electrophilic substitution reaction on the benzene ring and during the reaction an intermediate will also be formed in which there will be positive charge distributed in the benzene
These electrophile is generated when nitric acid is treated with sulphuric acid
As nitric acid is a strong oxidising agent, here in this case the oxidation state of nitrogen will change from +5 to +3
The reactions regarding the nitration of benzene is present in the file attached
Grass contains water and sheep need water.
Answer:
See explanation below
Explanation:
You are missing the structure, therefore, I will do an example with one that I found on another place to try to explain.
This acid mechanism always involves carbocations, and positive charges, never negative because we are in acidic mediums.
In the first step, the lone pairs of the oxigen from the epoxide, substract one hydrogen of the reactant.
Second step, the lone pairs of the oxygen from the reactant, do a nucleophylic attack to the carbon of the epoxide. In this case, it will do it to the most substitued carbon.
Then, in the third step by acid base equilibrium, the hydrogen from the reactant that attacked, is substracted from the molecule by a molecule of water (We are in acid medium, therefore, there is traces of water) and the final structure is formed.
Check picture for mechanism: