organic chemistry - Why does the Wurtz reaction form such an unstable compound with torsional strain?

What would be the product formed when 1-bromo-3-chlorocyclobutane with two equivalents of metallic sodium in ether?

I know that there would be a free radical formation and then it will form a compound whose bond line structure would look like a square with a diagonal.

But why is such an unstable compound being formed as there is a lot of torsional strain?

Answer

In the Wurtz coupling reaction, an alkyl halide first reacts with a metal in a one-electron transfer step to produce an alkyl radical which quickly reacts in a second electron transfer with the metal to form a carbanion. In the final step of the reaction, the carbanion displaces a halogen from a carbon-halogen bond by a $\ce{S_{N}2}$ process to form a carbon-carbon bond. In the case of 1-bromo-3-chlorocyclobutane two reaction pathways are possible, the carbanion could react intramolecularly to form bicyclobutane or intermolecularly to from a cyclobutane dimer. Considering the equation $$\ce{\Delta G = \Delta H - T \Delta S}$$ we would say that even though the $\ce{\Delta H}$ term is less favorable for bicyclobutane formation due to the increased ring strain, the change in entropy required to bring two separate molecules together to form the cyclobutane dimer overwhelms the enthalpic term and drives the reaction to proceed by the entropically more favorable intramolecular process.

Look at the cyclobutyl carbanion drawn in the figure below. The carbanion is ideally set up for an intramolecular $\ce{S_{N}2}$ reaction (backside displacement) on the carbon containing the chlorine diagonally situated across from it. Entropically, this is extremely favorable.

In summary, because 1) the carbanion and the chloride to be displaced are in the same molecule, 2) because they are so well positioned for the $\ce{S_{N}2}$ displacement reaction to occur and 3) because entropy strongly favors the unimolecular process (bicyclobutane formation) over the bimolecular process (cyclobutane dimer formation), bicyclobutane formation readily occurs.