Bicyclic ketone A rapidly equilibrates with a stereoisomer upon treatment with strong base, but ketone B does not. Explain why in a post with others in your group. Comment on the posts of at least two other students - have they correctly explained the difference in behavior between ketones A and B?

Consider the following reaction at equilibrium: c(s)+h2o(g)⇌co(g)+h2(g) predict whether the reaction will shift left, shift right, or remain unchanged upon each of the following disturbances. a) c is added to the reaction mixture. b) h2ois condensed and removed from the reaction mixture c) co is added to the reaction mixture d) h2 is removed from the reaction mixture.