In which of the following is the first resonating structure less stable compared to the second one?

Consider the following statements. Which of the following statement$(s)$ is/are correct?
$(a)$ $CH_2=CH-CH_2^+$ is more stable than $CH_3-CH^+-CH_3$.
$(b)$ Naphthalene has two types of $C-C$ bonds.
$(c)$ The structures shown are both permissible resonating structures.
$(d)$ The phenyl anion is less stable than the cyclohexadienyl anion shown.

The order of relative stability of the contributing structures is:
$I: CH_2=CH-CHO$
$II: ^+CH_2-CH=CH-O^-$
$III: ^-CH_2-CH=CH-O^+$
Choose the correct answer from the options given below:

Identify the correct stability order of the resonating structures.

Given below are two statements.
Statement $I :$ The dipole moment of $CH_3-CH=C(CH_3)-CH=O$ is greater than $CH_3-CH_2-CH_2-CH=O$.
Statement $II :$ $C_1-C_2$ bond length of $CH_3-CH=CH-CH=O$ is greater than $C_1-C_2$ bond length of $CH_3-CH_2-CH_2-CH=O$.
In the light of the above statements,choose the correct answer from the options given below $:$

Draw other resonance structures related to the following structure and find out whether the functional group present in the molecule is ortho,para directing or meta directing.