Draw the structures, including stereochemistry, of the two intermediates and the final product. Use wedge‑and‑dash bonds and hydrogens on chirality centers. The starting material is a disubstituted benzene. On carbon 1 of the ring, the substituent is a 6 carbon chain where there is a double bond between carbons 5 and 6. On carbon 3 of the ring, there is a 5 carbon chain with a double bond between carbons 4 and 5. The 5 carbon chain has a chiral center on carbon 2, with a wedged bond to hydrogen and a dashed bond to methyl. The starting material reacts with the Grubbs G 2 catalyst to form a mixture of two optically active compounds. The two intermediate react with H 2 and palladium on carbon to give a single optically active product.