Which of the following is not chiral: DCH2CH2CH2Cl, CH3CHDCH2Cl, CH3CHClCH2D, or CH3CH2CHDCl?
Ella AllenIn contrast to the other three molecules, which all have at least one carbon center bearing four different substituents, potentially producing two optical antipodes, the molecule above lacks a stereogenic center and has two carbons bearing the same substituent.
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Nolan AllenCH3CH2CHDCl
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- How would you find the number of diastereomers?
- When is a compound optically active?
- What do L-, D-, R-, and S- (in enantiomers) stand for?
- How can we separate enantiomers?
- How does one tell if a compound is optically active or inactive by looking at it? For examples: 1-4-dichloro-2-methylpentane and 1,2-dichloro-2-methylpentane
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