Chapter Tua. adicaotaoy o 1. Order the following carbon radicals from most stable to least stable....
Clapler lud. Ndullal Janity To 1. Order the following carbon radicals from most stable to least stable. در حال اجرا CHA
order the following carbon radicals from most stable to least
stable
(1&2)
1. Order the following carbon radicals from most stable to least stable. 5 3 2 2. Complete the following reaction scheme. "What goes over the arrow?" Write your answers in the spaces provided below. MgBr Br E Br ОН MgCl CI F G В Н Br Reagents required for the above reactions: F. А. G. В. Н. С. I. D. J. E. (
Arrange the following radicals in order of increasing stability
(least stable to most stable)
Arrange the following radicals in order of increasing stability (least stable to most stable). Least stable Most stable
Arrange the following radicals in order of increasing stability, with 1 being the least stable and 7 being the most stable.23.1 (3).png23.1 (2).png23.1 (1).png
2. Rank the following radicals in decreasing order of stability (1-most stable, 5-least stable): CH2 CH3 (CH3)2Ć (CH3)2CH CH3CH2
6. Rank these carbon radicals from most stable to least stable: H C H Н—с—н (X) (W) н C H (z) (Y) 4. The equilibrium constant (Kea) for the conversion of A to B is 12.4. Which substance, A or B, is present in the larger amount at equilibrium? Next, solve for AG and decide on the spontaneity of the conversion. В A 8. What make this a chiral molecule? O H2N CH C OH CH2 HN-
Rank the following radicals in order of decreasing stability (most stable to least stable 11 III TV III > I > I > IV III > | > | > IV Ill > IV> || >1 IV>]> || > III II >> III > IV
Sort the radicals below from least stable (1) to most stable (3). identify the reagents a-c in the following scheme Predict the products of the reactions below
11. Arrange the following radicals in order of increasing stability (where 1 -least stable and 4- most stable). Explain your reasoning. Sob to Explain your reasoning:
1. Rank the following carbocations in order from most stable (1) to least stable (4). o ó no 8 2. Consider the following carbocation. Would this carbocation undergo a rearrangement? If so, show the mechanism (curved arrows) for the rearrangement (including the rearranged cation that is the product of your curved arrows) and explain why it happens. If not, explain why it would not rearrange.