Answer:
a new scientific discovery that benefits the environment
B . microscope
this is the answer .
Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Answer:
As for your question, I know to forget to put the options, specifically that your question is incomplete.
Explanation:
Although it could help you by telling you that always a reaction that seeks to balance the pH, and achieve neutrality ... It is necessary to achieve a concentration of OH equal to that of H +, in this way the hydroxyl and the protons.
