Answer:
a.Phenols have the ability to spread out the negative charge that forms.
Explanation:
This happens because of the aromatic ring the phenols have. When loosing the proton, the anion formed have different resonance isomers due to the double bonds in the aromatic ring. This resonance makes the anion more stable and prevents the reaction going backwards.
On the other hand, regular alcohol doesn't have resonace and the reaction of loosing the proton goes leftward and righward: is in equilibrium.
That equilibrium decreases the acidity of the alcohol.
The density of an object or quantity of matter is its mass divided by its volume.
Answer:
The gain in mass by the negative electrode is the same as the loss in mass by the positive electrode. So the copper deposited on the negative electrode must be the same copper ions that are lost from the positive electrode.
The enol carbon or ∝-carbon nucleophile attacks at molecular bromine in the acid-catalyzed α-bromination of a ketone
Treatment of ketones with bromine in the presence of acid will results in formation of a new C-Br bond at the alpha position. The purpose of the acid is to catalysed formation of the enol from ketone , which is active nucleophile in the reaction. This reaction is called haloform reaction which is used to identify the methyl substituted ketone in the presence of aldehyde.
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