Chapter 2: 44P (page 140)
Compare the relative acidity of 1-molar aqueous solutions of the following acids.
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Chapter 2: 44P (page 140)
Compare the relative acidity of 1-molar aqueous solutions of the following acids.
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The following compounds can all react as bases.

Predict the products of the following acid-base reactions.
(a)

(b)

(c)

(d)

(e)

(f)

(g)

(h)

Like nitrogen and carbon, oxygen also shows this same hybridization effect on acidity. Both of the following compounds can lose a proton from a positively charged oxygen with three bonds to give a conjugate base containing a neutral oxygen with two bonds. One of these structures has pKa = -2.4 , while the other has pKa = -8.0.

Each of these compounds can react as an electrophile. In each case, use curved arrows to show how the electrophile would react with strong nucleophile sodium ethoxide, Na+ - OCH2CH3.
(a)

(b)
NH+4
(c)
CH3CH2Br
(d)
BH3
(e)
CH3COOH
(f)

Question: Circle the functional groups in the following structures. State to which class (or classes) of compounds the structure belongs.
(a)

(b)

(c)

(d)

(e)

(f)

(g)

(h)

(i)

(j)

(k)

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