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The maximum number of possible isomers (including stereoisomers) which may be formed on mono-bromination of $1-$methylcyclohex$-1-$ene using $Br_2$ and $UV$ light is. . . . . .

The most stable canonical structure of the given molecule is:

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Identify the total number of compounds containing at least one chiral carbon atom from the following list:
$1$. $2-$methylcyclohexanone
$2$. Cyclopentane$-1,3-$dione
$3$. $CH_3-CH_2-CH(NO_2)-COOH$
$4$. $CH_3-CH(I)-CH_2-NO_2$
$5$. $CH_3-CH_2-CH(OH)-CH_2OH$
$6$. $CH_3-CH_2-CH(I)-C_2H_5$

Which of the following structures has an $R$-configuration at the chiral center?

Which of the following conformers for ethylene glycol is most stable?

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