
1. Rank the following carbocations in order of increasing stability. “1” is the least stable, “4”...
Rank the following carbocations in order of increasing stability. “l” is the least stable, “4” is the most stable. (2 pts) or od ano CH3
Rank the following carbocations in order of increasing
stability. “1” is the least stable, “4” is the most stable
or ot an CH3 or
1. Rank the following carbocations in order of increasing stability. "I" is the least stable, "4" is the most stable. (2 pts) or and an ove сна
Rank the following carbocations in increasing order of
stability. (1 = least stable)
3. (5 points) Rank the following carbocations in increasing order of stability. (1 = least stable) eg og Å
1. (4 pts) Rank each of the following carbocations in order of stability (1 most stable and 4 least stable). н н сH н Н,с Н,с" H сH; CH3 Hас- H 2. (6 pts total; 2 pts each) Complete the following transformations by indicating the reactant structure or the major organic product(s). Place your answer(s) in the space provided. Be certain to indicate stereochemistry where applicable. Cl2 Он cat. H2SO H-о Br Br conc. HBra) сн сна 3. (10 pts...
Rank the following carbocations in order of decreasing stability. Most Stable Least Stable Least Stable
Rank the following carbocations in order of decreasing stability. Most Stable Least Stable Least Stable
Rank the following carbocations in order of decreasing stability Most Stable Least Stable og ở bu
Rank the following carbocations in order of increasing stability. CHCI CH -CHCI C–CH CH C1 CH I II III a. (least stable) I < II < III (most stable) b. (least stable) II < I < III (most stable) c. (least stable) III < I < II (most stable) d. (least stable) III < II < I (most stable) e. (least stable) I < III < II (most stable) f. (least stable) II < III < I (most stable)
2. Carbocation stability: Rank the following carbocations from the most stable to the least stable. + (a) (b) (c) (d)