The X-ray analysis confirms the structure of the 12-methylene tautomer
formed by the acid catalysis of 6-fluoro- ,2,3,4-tetrahydro-7,12-dime
thylbenz-[a]anthracene. The central C ring is in a boat conformation,
with the result that the molecule is bent about a line through atoms C
(7) and C(12) with a dihedral angle of 32.5-degrees. The cyclohexene A
ring is in a half-chair conformation.