Question
KBr
m-nitrobenzoic
benzophenone
3. Look up and record the solubility in water for each of your three compounds 4. Define pKa and list the pKa of each of your
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Answer #1

3.

--> KBr is highly soluble in water. Because, It is ionic compound and ionizes to corresponding anion and cation. These ions gets hydrated in water and make KBr soluble in Water.

KBr -----------------> K+ (aq) + Br- (aq)

--> Since m-nitrobenzoic acid is a organic acid, m-nitrobenzoic acid is sparingly soluble in water. The solubility of m-nitrobenzoic acid in water is 0.24g/100 mL only. The polarity of m-nitrobenzoic acid less compare to KBr.

--> Since benzophenone is nonpolar in nature it will not dissolve in water like KBr and Benzoic acid. It is insoluble in water, but, soluble in nonpolar solvents like hexane, benzene etc.

4.

In KBr, Br- is very weak conjugate base of HBr which is very strong acid. Because of this, when KBr is dissolved in water the Br- wil not react with water and do not disturb the ionic product of the water. So, it is not possible to find pKa value for KBr.

--->

The pKa value for m-nitrobenzoic acid is 3.47 in water.  

Since the dissociation constant is 3.48 x 10-4.

--->

Since benzophenone is insoluble in water determination of pKa for benzophenone is not possible.

5.

In general organic acids are weak. so, produce strong conjugate bases. If pH of solution decreases, the solubility will decreases. This is due to, reaction of strong conjugate base with protons and forms undissociated acid which is insoluble.

If the pH increases, the deprotonation of organic acid increases, the OH- ions rapidly reacts with protons released from acid and drives solubility of organic acid by shifting dissociation in forward direction.

6.

Due to strong polar polar and nonpolar-nonpolar interactions, the polar molecule get dissolved in polar solvents and non polar molecules get dissolved in nonpolar solvents.   

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