This video discusses the acidity of organic compounds such as alcohols, phenols, amines, ammonium ions, alkynes, alkenes, thiols, aldehydes, ketones, esters, and carboxylic acids such as acetic acid. This video also provides the pKa values of most compounds presented in this video. It shows how to tell which compound is the stronger acid. Topics include electron donating and electron withdrawing groups, inductive effect, resonance stabilization of the conjugate base.
Examples include the acidity of the following compounds:
CH3OH, H2O, ethanol, isopropanol, tert-butanol
acetylene, ethene, and ethane
chloroacetic acid, fluoroacetic acid, bromoacetic acid,
benzoic acid, p-nitrobenzoic acid, iodoacetic acid
Hydronium ion, protonated ethanol ion, methyl ammonium,
CH4, NH3, H2O, HF, HCl, HBr, HI
Aniline, p-nitroaniline, p-methoxyaniline, diethyl amine,
Tagged under: acidity alcohols,acidity phenols,pka,acetic acid pka,acidity alkynes,pka acidity,acidity carboxylic acids,acidity,alkenes,ketones,aldehydes,thiols,alkynes,alcohols,phenols,carboxylic acid,acetylene pka,ethanol pka,CH3OH pka,isopropanol acidity,electron donating group,electron withdrawing groups,resonance stabilization conjugate base
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