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:
C. 3.40 ppm, singlet
Explanation:
Given the information from the question .we have to select the best representation for represents the predicted approximate chemical shift and coupling for hydrogen(s). In this case, there is no neighboring hydrogen .Thus there won’t be any split .the best option answer is C. 3.40 ppm, singlet . Therefore the correct answer or option is C. 3.40 ppm, singlet.
Answer: The solution will remain yellow.
Explanation:
A triple bonded carbon is called an alkyne. (with a y, e for double bond, a for single bond)
