What is the decreasing order of nucleophilicity for the following nucleophiles?
$A = CH_3COO^-$
$B = CH_3O^-$
$C = CN^-$
$D = CH_3-C_6H_4-SO_3^-$

Which of the following gives the highest yield of $2$-pentene upon reaction with $C_2H_5ONa/C_2H_5OH$?

The product $A$ of the following sequence of reactions is:
Ethylbenzene $\xrightarrow[(b) Cl_2, \Delta]{(a) Br_2, Fe}$ $\xrightarrow{(c) alc. KOH} 'A' \text{ (Major product)}$

The mechanism of $S_{N}1$ reaction is given as:
$R-X$ $\rightarrow R^{\oplus} X^{\ominus}$ $\rightarrow R^{\oplus} | X^{\ominus}$ $\xrightarrow{Y^{\ominus}} R-Y + X^{\ominus}$
(Ion pair) (Solvent separated ion pair)
$A$ student writes general characteristics based on the given mechanism as:
$(a)$ The reaction is favoured by weak nucleophiles
$(b)$ $R^{\oplus}$ would be easily formed if the substituents are bulky
$(c)$ The reaction is accompanied by racemization
$(d)$ The reaction is favoured by non-polar solvents.
Which observations are correct?

Predict the product for the following reaction:
$\xrightarrow[\Delta]{alc. \ KOH}$ product

$1$-chloroapocamphane is a bridgehead halide. Which of the following statements about its reactivity toward $AgNO_3$ is true?