Why are secondary and tertiary amines less soluble than primary amines of similar molecular size?
Because they can create fewer hydrogen bonds with the solvent in protic solvents, secondary and tertiary amines are less soluble in them.
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Secondary and tertiary amines have weaker hydrogen bonding capability compared to primary amines due to the absence of NH hydrogen atoms. This results in lower solubility in polar solvents like water.
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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.

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