3.4: In-Text References
- Page ID
- 354353
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- Recall that this is not the case for \(\mathrm{sp}^{2}\) or \(\mathrm{sp}\) hybridized carbon, which also form pi bonds, where the orbital overlap is destroyed by rotation. Therefore, as we will see later, a much higher input of energy is required for compounds with pi bonds to rotate the bonding carbons relative to each other. ↵
- See Chapter \(1\) and Chapter \(4\) in CLUE text. ↵
- https://en.Wikipedia.org/wiki/Tartaric_acid ↵
- Wikipedia on fluoxetine: https://en.Wikipedia.org/wiki/Fluoxetine ↵