Page 4 Flashcards

1
Q

What are constitutional isomers?

A

A: Compounds with the same molecular formula but different connectivity of atoms.

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2
Q

What are stereoisomers?

A

A: Compounds with the same molecular formula and connectivity but differ in the spatial arrangement of atoms

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3
Q

Give an example of constitutional isomers from the slide.

A

A: 2-methylpentane and 3-methylpentane.

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4
Q

Provide an example of stereoisomers from the slide.

A

A: Cis-1,2-dimethylcyclopentane and trans-1,2-dimethylcyclopentane.

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5
Q

What distinguishes cis-1,2-dimethylcyclopentane from trans-1,2-dimethylcyclopentane?

A

A: The spatial arrangement of the methyl groups: cis has them on the same side, while trans has them on opposite sides.

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6
Q

How do the names of stereoisomers differ?

A

A: Stereoisomers have the same name except for a prefix like cis or trans.

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7
Q

What do constitutional isomers and stereoisomers have in common?

A

A: Both have the same molecular formula.

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8
Q
A
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