CHEM 2323 Study Guide - Nucleophile, Hydrogenation, Ketone
Document Summary
Electrons in the tbondislooselyheldsinceitis furtheraway astrong electrophilecanpulltheelectrons to form anewbond making a carbocation. If doublebond is asymmetrical wemustworryaboutthedirection of addition e fe nu or nuiee e. 8. 3 rulesfor directionof addition markovnikov"srule original intheaddition ofan acidto a c c the hydrogenoftheacidattachesitselftothecarbonthat holds greater of hydrogens. Modern intheadditionof e to a c c theadditiongivesthemorestable of thetwopossible carbocations latets so carbocation stability determines selectivity. I ac e c the dilute at so g. I on 2 t "t city h on c it i. Hgload tho ii s ca spity on h y mechanism. Igor o toagone electrophilicattack mercuriniumion wateropensring yff 8a i gg. Alsogetenantiomer wehaveviolated neversw2on 30 us 2 carbon butit"s becausethis sushas snl character git gin a no say cats as. Rbett o h s rbi o o n migrates. Electrophilic addition of hox formshalohydrins t c io present got ph a. I c y y man 3 1,4 y"s orientation maintained.
