The reaction is an example of Friedel-Crafts acylation. The acylium ion (\(\text{RCO}^+\)) generated by the reaction of acyl chloride with \(\text{AlCl}_3\) acts as an electrophile and attacks benzene to form the acylated product.
\[ 6(-C=O)-C=O \]
Thus, the major product is:
\[ P = 6(-C=O)(-COPh) \]
Draw the structure of the major monohalo product for each of the following reactions:
Propene to 1-Iodopropane
Br\(_2\)/CS\(_2\)
Total number of nucleophiles from the following is: \(\text{NH}_3, PhSH, (H_3C_2S)_2, H_2C = CH_2, OH−, H_3O+, (CH_3)_2CO, NCH_3\)
In the following substitution reaction: