Hey! please help meee :-) i'm so close to being done
2 answers:
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Answer:
See explanation below
Explanation:
You forgot to put the picture to do so. In this case, I manage to find one, and I hope is the one you are looking for. If not, then post it again and I'll gladly help you out again.
According to the picture with the answer, we have a cyclohexane with 4 methyl groups there. Two of them are facing towards the molecule with a darker bond. This means that the alkyl bromide, should have a bromine in one of the bonds, and in order to produce an E2 reaction, this bromine should be facing in the opposite direction of the methyl groups which are facing towards. This is because an E2 reaction occurs with the less steric hindrance in the molecule. If the bromine is in the same direction as the methyl group, it will cause a lot more of work to do a reaction, and therefore, an E2 reaction. I will promote instead a E1 or a sustitution product.
Therefore the alkyl bromide should be like the one in the picture 2.
Answer:
Explanation:
first write the equilibrium equaion ,
⇄
assuming degree of dissociation =1/10;
and initial concentraion of =c;
At equlibrium ;
concentration of
is very small so
can be neglected
and equation is;
=
composiion ;