newman projection : conformational view along a carbon-carbon bond

14
H 3 C Conformations: 3-D arrangements of atoms in a molecule from rotation/twisting about single bonds Newman projection: conformational view along a carbon-carbon bond H 3 C H 3 C H 3 C H 3 C cp qz

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Newman projection : conformational view along a carbon-carbon bond. Conformations : 3-D arrangements of atoms in a molecule from rotation/twisting about single bonds. qz. cp. Conformations. - PowerPoint PPT Presentation

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Page 1: Newman projection :  conformational view  along a carbon-carbon bond

H3C

Conformations: 3-D arrangements of atoms in a molecule from rotation/twisting about single bonds

Newman projection: conformational view along a carbon-carbon bond

H3CH3C

H3CH3C

cp qz

Page 2: Newman projection :  conformational view  along a carbon-carbon bond

ConformationsStaggered conformation: atoms/groups on 1 carbon are as far apart as possible from the atoms/groups on adjacent carbon

H

H H

H H

H

= 60o

cp qz

Page 3: Newman projection :  conformational view  along a carbon-carbon bond

ConformationsEclipsed conformation: atoms/groups on 1-C in

closet approach to atoms/groups on adjacent C

H

H H

H

HH

same plane= 0o

cp qz

Page 4: Newman projection :  conformational view  along a carbon-carbon bond

ConformationsTorsional strain or eclipsed interaction strainstrain (E) arises from nonbonded atoms rotate from

staggered to eclipsed conformations

+12.6 kJ/mol

cp qz

Page 5: Newman projection :  conformational view  along a carbon-carbon bond

Conformations

Ethane as a function of dihedral angle

cp qz

Page 6: Newman projection :  conformational view  along a carbon-carbon bond

Conformations

anti conformation– a conformation about a single bond in which the

groups lie at a dihedral angle of 180°

CH3

H H

H H

CH3

cp qz

Page 7: Newman projection :  conformational view  along a carbon-carbon bond

ConformationsSteric strain (nonbonded interaction strain):

when atoms separated by 4 (more) bonds are forced closer

Angle strain:when a bond angle must compressed or expanded from 109.5o

calculate total strain - determine the lowest energy conformation ( molecular mechanics )

cp qz

Page 8: Newman projection :  conformational view  along a carbon-carbon bond

Conformations

– conformations of butane as a function of dihedral angle

cp qz

Page 9: Newman projection :  conformational view  along a carbon-carbon bond

Cyclopropane

angle strain: bond angles compressed (109.5° 60°)torsional strain: all 6Hs eclipsed

strain energy highH

H

H

H

H

H

cp qz

Page 10: Newman projection :  conformational view  along a carbon-carbon bond

Cyclobutane

puckering torsional strain slight angle strain

H

H

H

H

H H

H H

H H

HH

H

H

HH

net - puckered (butterfly) minimum energy conformation

but strain energy highcp qz

Page 11: Newman projection :  conformational view  along a carbon-carbon bond

Cyclopentane

“envelope” - torsional strain slightly angle strain

envelope ~ 1/4th strain energy of cyclopropane

H

H

H

H

H H

H

H HH

H H

H

HH

H

H

H

H

H

cp qz

Page 12: Newman projection :  conformational view  along a carbon-carbon bond

Cyclohexane - chair conformationBond bond angles - 110.9° StaggeredNo angle or torsional strain

six Hs are axial and six equatorial

H

H

H

H

H

H

HHH

H H H

cp qz

Page 13: Newman projection :  conformational view  along a carbon-carbon bond

cyclohexane 2 equivalent chair conformations

Flip converts

6 equatorial 6 axial

6 axial Hs in one chair 6 equatorial Hs in other

H

H

H

H

H

H

HHH

H HH

H

HH

H

H

H

H H

H H H

H?

cp qz

Page 14: Newman projection :  conformational view  along a carbon-carbon bond

Equatorial and axial methyl conformations

Methylcyclohexane

CH3H

HH

H

H

H

HH H

HH

H

H

HH

H

H

HHH

HCH3

H +7.28 kJ/mol

94 / 6

cp qz