Guided course 01:49Provide the correct common and IUPAC name.Johnny Betancourt2036views29rank14comments
Guided course 00:59Provide the correct common and IUPAC name.Johnny Betancourt1801views27rank11comments
Textbook QuestionPredict which member of each pair has the higher boiling point, and explain the reasons for your predictions. (a) hexan-1-ol or 3,3-dimethylbutan-1-ol (b) hexan-2-one or hexan-2-ol719views
Textbook QuestionPredict which member of each pair will be more soluble in water. Explain the reasons for your answers. (a) hexan-1-ol or cyclohexanol (b) heptan-1-ol or 4-methylphenol (c) 3-ethylhexan-3-ol or octan-2-ol (d) hexan-2-ol or cyclooctane-1,4-diol (e) or 734views
Textbook QuestionDraw the structures of the following compounds. (Includes both new and old names.) (d) 3-cyclopentylhexan-3-ol (e) meso-2,4-pentanediol497views
Textbook QuestionPredict which member of each pair will be more acidic. Explain your answers. (d) 2,2-dichloropropan-1-ol or 2,2-difluoropropan-1-ol418views
Textbook QuestionPredict which member of each pair will be more acidic. Explain your answers. (c) 2-chloroethanol or 2,2-dichloroethanol537views
Textbook QuestionPredict which member of each pair is more acidic, and explain the reasons for your predictions. (b) cyclohexanol or cyclohexanethiol484views
Textbook QuestionPredict which member of each pair is more acidic, and explain the reasons for your predictions. (a) cyclopentanol or 3-chlorophenol451views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group? (b) NaOH343views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group? (c) NaCN347views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group? (e)324views
Textbook Question(•) The following molecules were named incorrectly according to IUPAC nomenclature. Give the correct name of these compounds.(a) 3-oxo-5-methylhexan-2-ol341views
Textbook Question(••) Draw the correct structure from the following IUPAC names:(a) (4R,2Z)-4-methylhex-2-en-1-ol283views
Textbook Question(••) Draw the correct structure from the following IUPAC names:(c) (1S,4R)-4-bromocyclohex-2-en-1-ol306views
Textbook QuestionDraw a condensed structure for each of the following:g. 1-bromo-1-pentyneh. 5-methyl-2-cyclohexenol263views
Textbook QuestionGive a systematic (IUPAC) name for each alcohol. Classify each as primary, secondary, or tertiary.(f) <IMAGE>(g) <IMAGE>282views
Textbook QuestionGive a systematic (IUPAC) name for each diol(a) CH3CH(OH)(CH2)4CH(OH)C(CH3)3(b) HO-(CH2)8-OH(c) <IMAGE>498views
Textbook QuestionPredict which member of each group is most soluble in water, and explain the reasons for your predictions.(a) butan-1-ol, pentan-1-ol, or propan-2-ol271views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group?(d) Et₃N309views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group?(a) <IMAGE>285views
Textbook QuestionPropose mechanisms to show the interchange of protons between ethanol molecules under (a) acid catalysis. (b) base catalysis.411views