(a)
Interpretation: All the stereogenic centers in the given compound are to be located.
Concept introduction: An atom or a group bearing four different atoms or groups which produces stereoisomers on interchange of any two groups are stereogenic centers.
(b)
Interpretation: The stereogenic centers due to carbon-carbon double bond in the given compound are to be located.
Concept introduction: An atom or a group bearing four different atoms or groups which produces stereoisomers on interchange of any two groups are stereogenic centers.
(c)
Interpretation: Maximum number of stereoisomers is to be predicted.
Concept introduction: An atom or a group bearing four different atoms or groups which produces stereoisomers on interchange of any two groups are stereogenic centers.
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Organic Chemistry
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- I want to answer all branchesarrow_forward9.a. Circle all the appropriate terms. t-Bu The two molecules drawn above are enantiomers optically active enantiomers superimposable 9.b. Circle all the appropriate terms. diastereomers not optically active H optically active Bull.... H₂CH... Br -CH3 The two molecules drawn above are Me H diastereomers not optically active superimposable Me chiral meso not superimposable H3C- H ....... chiral meso H ...III\CH3 Br not superimposable Cl achiral -t-Bu identical achiral identical 3arrow_forwardLocate the stereogenic center in each compound and draw both enantiomers.arrow_forward
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