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Lecture 8- Stereochemistry 1/4

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Total cards: 13•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Draw the family tree of isomers

Back (Answer)

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#2
Front (Question)

definition of a structural isomer

Back (Answer)

different compounds with the same molecular formula (but a different structural formula).

#3
Front (Question)

Draw two structural isomers with the molecular formular C4H10

Back (Answer)

Card back image
#4
Front (Question)

What is a stereoisomer?

Back (Answer)

Same constitutions, same formula, different spatial arrangement.

#5
Front (Question)

What is a conformational isomer?

Back (Answer)

Different arrangement of atoms due to bond rotation

#6
Front (Question)

What bonds allow for conformational isomers?

Back (Answer)

sigma bonds

#7
Front (Question)

Draw the two types of confirmation of ethane using the Newman projection. Name them

Back (Answer)

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#8
Front (Question)

Is the staggered or eclipsed confirmation preferred?

Back (Answer)

Staggered because it is in a lower energy due to the C-H bonds being further from each other- minimises repulsion between electrons.

#9
Front (Question)

Draw a chair cyclohexane showing the equatorial and axial bonds

Back (Answer)

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#10
Front (Question)

An axial bond is drawn upwards for every carbon that points …….. and downwards for every carbon that points ………….

Back (Answer)

up down

#11
Front (Question)

How do you draw equatorial bonds?

Back (Answer)

109.5 degrees from the axial bonds. If axial bond is up, equatorial is down and vice versa.

#12
Front (Question)

Draw ring flipping for this molecule.

Card front image
Back (Answer)

Card back image
#13
Front (Question)

In terms of ring flipping, is it preferred for groups of higher molecular mass to be in axial positions or equatorial?

Back (Answer)

Equatorial. Axial is higher in energy- groups in axial are closer together.