Answer:
trans-1,3-pentadiene is more stable than 1,4-pentadiene due to presence of a conjugated double bond.
Explanation:
Here, 
H(hydrogenated pdt.) is same for both 1,4-pentadiene and 1,3-pentadiene as they both produce pentane after hydrogenation
H(diene) depends on stability of diene.
More stable a diene, lesser will be it's H(diene) value (more neagtive).
trans-1,3-pentadiene is more stable than 1,4-pentadiene due to presence of a conjugated double bond.
Hence,
is higher (less negative) for trans-1,3-pentadiene
Answer:

Explanation:
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In this case, for this neutralization reaction, it is possible to realize that one the neutralization products is water (pH=7) and the other one is the salt coming up from the cation of the NaOH and the anion of the HI:

Moreover, since the solubility of NaI is large in water, we infer it remains aqueous whereas the water is maintained as liquid:

Which is also balanced as the number of atoms of all the elements is the same at both sides.
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Phosgene on reacting with <span>phenylmagnesium bromide generates
benzoyl chloride.
Since, </span>phenylmagnesium bromide is added in excess. It would further react with benzoyl chloride to form
benzophenone.
Benzophenone on further reacting with phenylmagnesium bromide, and aqueous treatment, gives
triphenylmethanol.
Entire reaction pathways is shown below:
Ne is isoelectronic with Na+ ion.
Answer: Fluorine
Explanation: It belongs in the same group as Bromine