Na releases 1 electron to be stable
Cl requires 1 electron to be stable
both are ionic bonded to be stable
The answer is the 3rd one
Benzene is more volatile.
Answer:
Explanation is in the answer
Explanation:
The pH of the buffer solution does not change appreciably because the strong acid (free H⁺) reacts with conjugate base of buffer producing more weak acid. pH formula of buffers is (Henderson-Hasselbalch formula):
pH = pKa + log ( [A⁻] / [HA] )
The addition of strong acid decreases [A⁻] increasing [HA]. pH change just in the log of the ratio of [A⁻] with [HA], that is a real little effect over pH of the buffer solution.
Answer:
Benzaldehyde is less electrophilic than acetaldehyde
Explanation:
Electrophilicity of carbonyl carbon depends on it's positive charge density.
In benzaldehyde, phenyl group can act as an electron donating group towards carbonyl group due to it's electron donating resonating effect.
In acetaldehyde, methyl group can act as an electron donating group towards carbonyl group due to it's electron donating inductive effect.
We know that resonating effect are more stronger than inductive effect.
Henece, it is expected that positive charge density on carbonyl carbon is much lower in benzaldehyde than acetaldehyde.
So, benzaldehyde is less electrophilic than acetaldehyde.
Resonating effect of phenyl group has been shown below.