subject
Chemistry, 17.12.2019 01:31 nihadsalim10

The reaction of butan-2-ol with concentrated aqueous hbr goes with partial racemization, giving more inversion than retention of configuration. propose a mechanism that accounts for racemization with excess inversion. (b) under the same conditions, an optically active sample of trans-2-bromocyclopentanol reacts with concentrated aqueous hbr to give an optically inactive product, (racemic) trans-1,2- dibromocyclopentane. propose a mechanism to show how this reaction goes with apparently complete retention of configuration, yet with racemization.

ansver
Answers: 3

Another question on Chemistry

question
Chemistry, 21.06.2019 20:00
Which object forms when a supergiant runs out of fuel? a red giant a black hole a white dwarf a neutron star
Answers: 1
question
Chemistry, 21.06.2019 22:50
Blank allows you to do calculations for situations in which only the amount of gas is constant a)boyle's law b)combined gas law c)ideal gas law d)dalton's law
Answers: 1
question
Chemistry, 22.06.2019 01:20
Match the acid base pairs by arranging the acid name with the conjugate base formula. hydrogen carbonate hydrogen phosphate carbonic acid read water sulfuric acid phosphoric acid a. co32- b. hso4- c. hco3- d. po43- e. h2po4- f. oh-
Answers: 1
question
Chemistry, 22.06.2019 03:30
Calcium chloride +gold(1) oxide—>
Answers: 1
You know the right answer?
The reaction of butan-2-ol with concentrated aqueous hbr goes with partial racemization, giving more...
Questions
question
Mathematics, 19.11.2020 21:00
question
Mathematics, 19.11.2020 21:00
question
Geography, 19.11.2020 21:00
question
Mathematics, 19.11.2020 21:00
question
Mathematics, 19.11.2020 21:00
Questions on the website: 13722363