The molecular structures of cis-2-butene and trans-2-butene are presented below:
cis-2-butene: \( \text{CH}_3 - \text{CH} = \text{CH} - \text{CH}_3 \) (Polar)
trans-2-butene: \( \text{H} - \text{CH} = \text{CH} - \text{CH}_3 \) (Non-Polar)
Cis-but-2-ene exhibits a greater dipole moment compared to trans-but-2-ene owing to the spatial orientation of its substituent groups. The cis arrangement leads to a resultant dipole moment, whereas the symmetrical trans arrangement causes the dipoles to cancel.
Consider the following reaction sequence.
Which of the following hydrocarbons reacts easily with MeMgBr to give methane? 