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.
Yes the answer is 1s22s22p63s23p64s23d5
<span>Solubility product constant (Ksp) is </span>applied to the saturated ionic solutions<span> which are in equilibrium with its
solid form. The solid is partially dissociated into its ions.</span><span>
For the BaF, the dissociation as follows;
BaF</span>₂(s) ⇄ Ba²⁺(aq)
+ 2F⁻(aq)
<span>
Hence,
Ksp = [Ba</span>²⁺(aq)] [F⁻(aq)]²
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