With reference to the indicated C–H bonds in the following compound:a.) Rank the C–H bonds in order of increasing bond strength. b.) Draw the radical resulting from cleavage of each C–H bond, andclassify it as 1°, 2°, or 3°. c.) Rank the radicals in order of increasing stability.d.) Rank the C–H bonds in order of increasing ease of H abstraction in aradical halogenation reaction.

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With reference to the indicated C–H bonds in the following compound:
a.) Rank the C–H bonds in order of increasing bond strength.

b.) Draw the radical resulting from cleavage of each C–H bond, and
classify it as 1°, 2°, or 3°.

c.) Rank the radicals in order of increasing stability.
d.) Rank the C–H bonds in order of increasing ease of H abstraction in a
radical halogenation reaction.

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