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Consider the acidity constants below to answer the following question(s). Which acid will be almost completely deprotonated by NaOH? phenol ethanol water not enough information is provided to answer the question. Consider the acidity constants below to answer the following question(s).

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Pyridine can be modified by attaching different groups on the asterisk. As a result of this, some properties of the compound may vary. One property that is affected is the acidity of the conjugate bases. The acid dissociation constants of the conjugate acids are given in the table below.

Group Substituted in Asterisk	K_aof Conjugate Acid
NO₂
Cl
H
CH₃

Suppose each conjugate acid is dissolved in water to yield a 0.050 M solution. Which solution would have the highest pH?

teallocust47

1. Which Base is stronger, the conjugate base of methane or theconjugate base of ethane?

2. Is sodium ethoxide( NaOCH2CH3) a strong enough base todeprotonate acetylene?

3. Is sodium ethoxide able to deprotonate methanol?

4. Is sodium methoxide able to deprotonate ethanol?

5. Which halide ion is NOT able to deprotonate HBr?

6. The acetylide ion cannot come into contact with water or itwill deprrotonate. As such, will the acetylide iondeprotonate ammonia?

7. Is methanethiol a strong enough acid to deprotonatewater?

8. There is a mixture of equal parts water, methanol, andethanol. A very soluble unknown base is added to thesolution in excess. The conjugate acid of the unknownbase has a pKa of 15.5. Identify all components of themixture that will be deprotonated.

9. Identify any one compound from the table that will beprotonated by acetic acid,

10. Identify any one compound from the table that will bedeprotonated by the hydride ion H-.

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Consider the acidity constants below to answer the following question(s). Which acid will be almost completely deprotonated by NaOH? phenol ethanol water not enough information is provided to answer the question. Consider the acidity constants below to answer the following question(s).

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