Answer:
1) HNO3/H2SO4, 2) CH3CH2CH2Cl/AlCl3
Explanation:
Benzene is a stable aromatic compound hence it undergoes substitution rather than addition reaction.
When benzene undergoes substitution reaction, the substituent introduced into the ring determines the position of the incoming electrophile.
If I want to synthesize m-nitropropylbenzene, I will first carry out the nitration of benzene using HNO3/H2SO4 since the -nitro group is a meta director. This is now followed by Friedel Craft's alkykation using CH3CH2CH2Cl/AlCl3.
Answer:
Anyone should be able to read the lab report, repeat the experiment, and get the same results. This is important for scientists. ... They help the scientists know what has been done before and how it was performed. This can help them design experiments for their own research
Answer:
Molarity= 1.69M
Explanation:
m= 14.8, Mm= 35, V= 0.25dm3, C= ?
Moles = m/M= C×V
Substitute and Simplify
m/M= C×V
14.8/35= C×0.25
C= 1.69M
Answer:
false
Explanation:
because it's just a physical change, the matter won't be changed.
Hope this might help you! I don't know if this is going to be right on everything, but it's a anwser
