Guided course 01:49Provide the correct common and IUPAC name.Johnny Betancourt2027views29rank14comments
Guided course 00:59Provide the correct common and IUPAC name.Johnny Betancourt1793views27rank11comments
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-ol715views
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 733views
Textbook QuestionDraw the structures of the following compounds. (Includes both new and old names.) (d) 3-cyclopentylhexan-3-ol (e) meso-2,4-pentanediol495views
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-dichloroethanol535views
Textbook QuestionPredict which member of each pair is more acidic, and explain the reasons for your predictions. (b) cyclohexanol or cyclohexanethiol483views
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) NaOH341views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group? (c) NaCN343views
Textbook QuestionWhich of the following bases would favorably deprotonate a hydroxyl group? (e)321views
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-ol282views
Textbook Question(••) Draw the correct structure from the following IUPAC names:(c) (1S,4R)-4-bromocyclohex-2-en-1-ol304views
Textbook QuestionDraw a condensed structure for each of the following:g. 1-bromo-1-pentyneh. 5-methyl-2-cyclohexenol260views
Textbook QuestionGive a systematic (IUPAC) name for each alcohol. Classify each as primary, secondary, or tertiary.(f) <IMAGE>(g) <IMAGE>281views
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>496views
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-ol270views
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>284views
Textbook QuestionPropose mechanisms to show the interchange of protons between ethanol molecules under (a) acid catalysis. (b) base catalysis.409views