Because it has no <span> stereogenic carbon centres.</span>
Answer:
in a chemical reaction of NaOH with H2O, after NaOH is completely disassociated, we will find Na+ and OH- ions in the solution. (option C).
Explanation:
In a reaction where NaOH is added to H2O.
NaOH is considered a strong base, this means that in an aqueous solution ( in water) it's able to completely disassociate in ions.
There will not remain any NaOH in the solution. This means option D is not correct.
The ions in which NaOH will disassociate are : NaOH → Na+ + OH-
These ions we will find in the solution.
Not only Na+ because NaOH is a strong base, so there will be a lot of OH- ions as well in solution.
This means in a chemical reaction of NaOH with H2O, after NaOH is completely disassociated, we will find Na+ and OH- ions in the solution.
2-bromo-1-chloro-4-nitrobenzene is being synthesized in following sequence:
Step 1: Chlorination of Benzene:
This is Halogenation reaction of benzene. In this step benzene is reacted with Chlorine gas in the presence of lewis acid (i.e. FeCl₃). This results in the formation of Chlorobenzene as shown in red step below.
Step 2: Nitration of Chlorobenzene:
The chlorine atom on benzene has a ortho para directing effect. Therefore, the nitration of chlorobenzene will yield para nitro chlorobenzene as shown in blue step below.
Step 3: Bromination of 1-chloro-4-nitrobenzene:
In this step bromination is done by reacting bromine in the presence of lewis acid. The chlorine being ortho para directing in nature and nitro group being meta directing in nature will direct the incoming Br⁺ (electrophile) to the desired location. Hence, 2-bromo-1-chloro-4-nitrobenzene is synthesized in good yield.