Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
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Answer:
Explanation:
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Answer:
on https://www.ck12.org/book/peoples-physics-concepts/section/20.1/
Explanation:
it shows for calcium 45 and maybe a possible equation on 3/4th's scroll down?
Is it multiple choice or anwser or each question
Answer:
Carbonyl
Explanation:
While the diagram is slightly unclear, the molecule most likely being shown is a carbonyl. A molecule is a carbonyl when there is a carbon double-bonded to an oxygen.
