Answer:
E 1: cyclohexene
Explanation:
This reaction is an example of the dehydration of cyclic alcohols. The reaction proceeds in the following steps;
1) The first step of the process is the protonation of the cyclohexanol by the acid. This now yields H2O^+ attached to the cyclohexane ring.
2) the water molecule, which a good leaving group now leaves yielding a carbocation. This now leaves a cyclohexane carbocation which is highly reactive.
3) A water molecule now abstracts a proton from the carbon adjacent to the carbocation leading to the formation of cyclohexene and the regeneration of the acid catalyst. This is an E1 mechanism because it proceeds via a carbocation intermediate and not a concerted transition state, hence the answer.
This is true otherwise cancer patients would have a hole in them and so would the hulk ;)
Answer:
107Ag has abundance of 51.7%
109Ag has abundance of 48.3%
Explanation: Please see attachment for explanation
Notice q=3/2, is half of the original q = 3(<span>1/2</span>)<span>t/28.8
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2NH4ClO4 --------> N2 + Cl2 + 2O2 + 4H2O
from reaction 2 mol 1 mol
given x mol 0.10 mol
Proportion:
<u>2 mol NH4ClO4 </u>= <u>1 mol Cl2</u>
x mol NH4ClO4 0.10 mol Cl2
x= (2*0.10)/1 = 0.20 mol NH4ClO4
