| 11. | It may be considered the conjugate acid of the azide anion, and is similarly analogous to the hydrohalic acids.
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| 12. | In these reactions the conjugate acid of the carbonyl group is a better electrophile than the neutral carbonyl group itself.
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| 13. | Some reagents are of high basicity ( pK a of conjugate acid around 17 ) but of modest but not negligible nucleophilicity.
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| 14. | The least reactive monomers have the largest pKa values for their corresponding conjugate acid and thus, require the most reactive initiator.
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| 15. | The pKa values for the conjugate acids of the carbanions formed from monomers can be used to deduce the reactivity of the monomer.
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| 16. | How do we deal with compounds such as Geranyl pyrophosphate which may exist in various conjugate acid / base forms under physiological conditions?
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| 17. | The addition of an H + ion to an ammonia molecule of the solvent creates its conjugate acid, the ammonium ion, NH.
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| 18. | This is because guanidinium is the conjugate acid of guanidine and is called the guanidinium cation, [ CH 6 N 3 ] +.
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| 19. | The corresponding conjugate base of each conjugate acid state also has a different base-dissociation equilibrium constant K b1 and K b2, respectively.
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| 20. | Their advantages for this are : they are very strong bases in many solvents and their conjugate acids are inert and non-HBD cations.
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