Arrange the following methyl halides in order of increasing C-X bond strength. S

Question

Arrange the following methyl halides in order of increasing C-X bond strength. Start with the C-X bond. CH3-F CH3-CL CH3-Br CH3-1 Arrange the following C-H bonds in order decreasing toward radical halogenations. Start with the most reactive C-H bond. (CH2)3C-H CH3CH -H (CH3)2CH-H CH3-H Arrange the following radicals in order of decreasing stability, Start with the most stable radical Arrange the following alcohols in order of decreasing reactivity toward nucleophilic substitution in either Start with the most reactive alcohol.

Explanation / Answer

19)A>B>C>D 20)D>C>B>A 21)B>A>C 22)A

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