Which of the following strategies is used while naming a cycloalkene?
A) The substituents are numbered first, and the numbering is continued in the direction where the double bond gets the lowest possible number.
B) The cyclic ring is broken down at one of the positions of the double bond, and the numbering is done as with the alkenes.
C) The double bond is numbered 1 and 2 in the direction where a substituent gets the lowest possible number.
D) The double bond is numbered 1 and 2 in the direction where a substituent gets the highest possible number.
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