




To determine the major product of the given reaction, let's analyze the provided structure and reaction conditions.
The starting material is a bicyclic compound with a double bond and axial hydrogens. The reaction is carried out at 150°C, indicating a possibility of a thermal rearrangement, particularly a Cope rearrangement or something similar due to the high temperature.
The compound is likely undergoing a conformational change leading to a more stable arrangement. The most feasible pathway is an internal rearrangement that relieves strain, possibly involving a ring expansion or contraction that forms a stable product.

In this scenario, the major product would involve the elimination of strain through a rearrangement to give a more favorable, stable product. This involves the migration of the double bond and hydrogens to achieve conjugation or relief of angle strain.
Conclusion: Based on the available options, the image above represents the correct major product of the reaction. This product is the result of the necessary rearrangement to achieve a lower energy state.
One mole of a monoatomic ideal gas starting from state A, goes through B and C to state D, as shown in the figure. Total change in entropy (in J K\(^{-1}\)) during this process is ............... 
The number of chiral carbon centers in the following molecule is ............... 
A tube fitted with a semipermeable membrane is dipped into 0.001 M NaCl solution at 300 K as shown in the figure. Assume density of the solvent and solution are the same. At equilibrium, the height of the liquid column \( h \) (in cm) is ......... 
An electron at rest is accelerated through 10 kV potential. The de Broglie wavelength (in A) of the electron is .............