UK NE r , CHEM 250 » Broyer University of Southern ¢ alifornia ol - sl Bn The pK, Short List % AL i H-Cl H % i %H }120 H—==H N 19 CHy ; R” “OH ; & i -8 ", 5 10 16 23 39 S0 ® 0 HZ.O.:/—\H"/;\ e H,O—H A (—] | Gonjugat@ Gonjugat@ base @Cl@ k acid %) % base ) [”306)“/\:@4’ If K, > 1, then the equation means —log K, which is useful because Ka ranges from 10°" — | 3. B [II;;O@][AG] K = P PRpiooks »d o KIH,O0| =K, = .07 [H-A] ‘which rearranged gives K[H; | =K, H-A] above describes a strong acid (favors product), but if K < 1 1t’s a weak acid. The term pK. 20 — 60 (approximately). 01 So pK. ranges from — dot structure for the molecules below. Be sure to draw all of the bonds, Draw a complete Lewis sible draw an important lone pairs, and formal charges. If multiple resonance structures areé pos (major) resonance form. tert-butyl alcohol (CH3)3COH acetic acid, CH3CO2H HoN?2 .. O >¢Q\’\ / \\ K ) H-N=N—H &J H_ “’lfl \ oV P \\\°(\/ o (/ "'@'—\/\ % (\ L ‘ el 15, w@ e € e ~ (— 4. Which compound is more soluble in water? Briefly explain your choice. CH3)2NH/ or CH3CH2CH3 / xZ N NR 9 j%m@\u}o@\“\sz&\‘\ \Q \Q@\ar
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CHEM 250 « Broyer Fall 2023 ¢ Page 4 of 4 University of Southern California ' ‘1o 1l - » M * DC ()\\ o Cirele the most acidic among the Hydrogens drawn in in the molecule bel i H g . 0 P J F @O SN H// @) 0O =0 e L & H 9. Provide a plausible acid base synthesis for this molecule. You may select from the following reagents.