Answers are grounded in this paper and cite their sources.
Complete analyses of the room-temperature proton spectra of cycloheptatriene (I) and its 7,7-bistrifuoromethyl derivative (II) have been achieved. Whereas the methylene protons of I are nonequivalent below about -140º, the trifluoromethyl groups in II remain equivalent on the n.m.r. time scale down to -185º. An explanation for this behavior is sought in the differences in the magnitudes of the vicinal coupling constants (J_(23)) of I and II. There is no change in any of the coupling constants of I over the temperature range from -70 to +115º. The n.m.r. evidence therefore gives no indication of the presence of norcaradiene in equilibrium with cycloheptatriene.
No takes yet. Share an insight, caveat, or question.
Lambert et al. (1965) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: