1. Redraw the structure below, showing both nonaromatic rings in chair conformations. Place the bridgehead hydrogen atoms in axial positions. Pay special attention to drawing the correct stereochemistry for all chirality centers, as shown in this structure. Assign each stereocenter as R or S. OOCH3 OH H2N

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1. Redraw the structure below, showing both nonaromatic rings in chair conformations.
Place the bridgehead hydrogen atoms in axial positions. Pay special attention to
drawing the correct stereochemistry for all chirality centers, as shown in this structure.
Assign each stereocenter as R or S.
„OCH3
"OH
OH
H2N
Transcribed Image Text:1. Redraw the structure below, showing both nonaromatic rings in chair conformations. Place the bridgehead hydrogen atoms in axial positions. Pay special attention to drawing the correct stereochemistry for all chirality centers, as shown in this structure. Assign each stereocenter as R or S. „OCH3 "OH OH H2N
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Aromatic compounds are the compound which follows the huckle rule for unsaturation and pie electrons. Huckel's rule is (4n+2)=pie electrons. If there are (4n+2) pie electrons then the compound is aromatic ('n'= Natural number represents rings present.). An aromatic structure is generally a planar ring containing structure. The name 'Aroma' represents the smell/odour having compounds.

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