exam three (conceptual)

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Last updated 4:06 PM on 10/19/26
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8 Terms

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aldehyde (overarching term)

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ketone (overarching term)

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acetone (type of ketone)

  • two bond angles are equal due to symmetry


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acetaldehyde (type of aldehyde)

  • all bond angles differ slightly


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Carbonyl group - Wikipedia

state the properties as well.

carbonyl group

geometry:

  • the carbonyl group in aldehyde and ketone are planar.

  • bond angles are ~120°, but are not identical bc the molecules aren’t symmetrical. (if both R groups are the same, then two bond angles are equal).


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polarity, resonance, and reactivity of carbonyl groups

Carbonyl group - Wikipedia
  • C=O is strongly polarized because Oxygen withdraws electron density from Carbon.

  • carboxyl is very electrophilic, so it’ll react with nucleophiles.


<img src="https://assets.knowt.com/user-attachments/c3157dfd-fd22-49fa-ad80-77d9a749f838.png" data-width="50%" data-align="center" alt="Carbonyl group - Wikipedia" style="display: block; width: 50%; margin-left: auto; margin-right: auto;"><ul><li><p>C=O is strongly polarized because Oxygen withdraws electron density from Carbon. </p></li><li><p>carboxyl is very electrophilic, so it’ll react with nucleophiles.</p></li></ul><p></p>
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organometallic reagents

compounds containing Carbon associated with a metal (Li, Mg, Cu).

  • carbon attached to a metal behaves as though it has sufficient negative charge


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is carbon electrophilic or nucleophilic?

Depends on circumstances:

carbonyl carbon (C=O): → δ+ → electrophilic

organometallic reagents: substantial negative charge → nucleophilic

<p><u>Depends on circumstances:</u></p><p>carbonyl carbon (C=O): → δ+ → <strong>electrophilic</strong></p><p>organometallic reagents: substantial negative charge → <strong>nucleophilic</strong></p>