Select the conjugate bases that will deprotonate water:
H-Cl pKa -7
CH3COO-H pKa 4.8
HO-H pKa 15.7
CH3CH2O-H pKa 16
HC?CH pKa 25
H-H pKa 35
H2N-H pKa 38
CH2=CH2 pKa 44
CH3-H pKa 50
All with pKa values that are higher than that of water (15.7) can deprotonate water. Thus the answers are:
CH3CH2O-H pKa 16
HC?CH pKa 25H-H pKa 35
H2N-H pKa 38
CH2=CH2 pKa 44
CH3-H pKa 50
Select the conjugate bases that will deprotonate water: H-Cl pKa -7 CH3COO-H pKa 4.8 HO-H pKa...
Select all that apply. Which of the following bases are strong enough to deprotonate CH3CH2CH2C CH (pKa 25), so that equilibrium favors the products' CH3ONa O H20 NH3 CH&Li NaCH2(CO)N(CH3)2 NaNH2 Select all that apply. Which of the following bases are strong enough to deprotonate CH3CH2CH2C CH (pKa 25), so that equilibrium favors the products' CH3ONa O H20 NH3 CH&Li NaCH2(CO)N(CH3)2 NaNH2
answer the problem show work thanks CH3 H2O + 1. H-C-CH-CH-CH2 CH3 CH C 2, CHy-CH2-CH-CHOHPCC 25°C 50-55°C + HNO H2SO4 он H2CrO4 CH,CHCH acetone, 35°c Et O 2150113H20 5. CH3(CH2)2MgBr+ CH3(CH2)sC(CH2)sCH3 Nall CH2-CHCH2l H2SO4 140°C 6. CH3CH2CH2OH 7. CHCH CHOH 1) LiAIH(O-t-Bu)3,-78°C 2) H20 8. CH,C-CI HBr 9. CH2 CH-CH-CH2 40°C 10. H3C CIH2 Benzene 100℃ H3C 1. LiAIH/Et2O 11. CH,CH2CH,COH 2. H,0 12. + CH,CH,cCI AIC Benzene, 80°C 13. Br2 heat CH3 AlcI 15. 25°C conc. H2SO4 NaBH4...
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