11. How many distinct monochlorinated products, including all stereoisomers, can result when methylcyclobutane is heated in the presence of Cl₂? (A) 2 (B) 6(C) 5 (D) 4(E) 3

7. Predict the specific rotation of the compound shown.(A) It is impossible to predict; it must be determined experimentally.(B) Because both asymmetric centers are R, the compound is dextrorotatory.(C) Because both asymmetric centers are S, the compound is dextrorotatory.(D) Zero; the compound is achiral.(E) Because this compound represents a racemic mixture, the compound is dextrorotatory.

11. How many distinct monochlorinated products, including all stereoisomers, can result when methylcyclobutane is heated in the presence of Cl₂?
(A) 2
(B) 6
(C) 5
(D) 4
(E) 3

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