
Let's analyze the reaction step-by-step:
1. Step 1: \({CH3CH2CH2Br} \xrightarrow[\Delta]{\text{alc. KOH}} {A}\)
Alcoholic KOH and heat promote elimination reactions. 1-Bromopropane reacts with alcoholic KOH to form propene (A) via a dehydrohalogenation reaction.
\({CH3CH2CH2Br} \xrightarrow[\Delta]{\text{alc. KOH}} {CH3CH=CH2(A)}\)
2. Step 2: \({A} \xrightarrow{\text{HBr}} {B}\)
Propene (A) reacts with HBr to form 2-bromopropane (B) as the major product according to Markovnikov's rule (the hydrogen atom adds to the carbon with more hydrogen atoms already attached).
\({CH3CH=CH2(A)} \xrightarrow{\text{HBr}} {CH3CHBrCH3(B)}\)
3. Step 3: \({B} \xrightarrow[\Delta]{\text{aq. KOH}} {C}\)
2-Bromopropane (B) reacts with aqueous KOH and heat to form propan-2-ol (C) via a nucleophilic substitution reaction (specifically, an S$_N$1 reaction is favored due to secondary alkyl halide and aqueous KOH).
\({CH3CHBrCH3(B)} \xrightarrow[\Delta]{\text{aq. KOH}} {CH3CH(OH)CH3(C)}\)
Therefore, the major product C is propan-2-ol.


Three identical heat conducting rods are connected in series as shown in the figure. The rods on the sides have thermal conductivity 2K while that in the middle has thermal conductivity K. The left end of the combination is maintained at temperature 3T and the right end at T. The rods are thermally insulated from outside. In steady state, temperature at the left junction is \(T_1\) and that at the right junction is \(T_2\). The ratio \(T_1 / T_2\) is 
