To answer questions 2, 3 and 6, optical rotation of (1R,2R)-(−)-1,2-Diaminocyclohexane[α]20/D −10.36°, c = 5To answer question 5, optical rotation of the synthesized diimine (Jacob’s ligand) [α]D20= – 315° (c=1, CH2Cl2).1)Draw the structure of 1R,2R)-(−)- 1,2-Diaminocyclohexane2) Discuss the optical rotation value obtained for both racemic 1,2-diaminocyclohexane and (1R,2R)-(−)- 1,2-Diaminocyclohexane.3) Predict the optical rotation value of (1S,2S)-1,2- Diaminocyclohexane.4) Are the melting points of racemic 1,2-diamino cyclohexane and (1R,2R)-(−)- 1,2-Diaminocyclohexane the same ? Explain.5) Define enantiomeric excess. Calculate it for the synthesized diimine (Jacob’sligand).6) Was the resolution of racemic 1,2-Diaminocyclohexane successful? Explain. . WITH topgradeassignments.org AND GET AN AMAZING DISCOUNT!The post To answer questions 2, 3 and 6, optical rotation of ( 1 R ,2 R )-()-1,2-Diaminocyclohexane []20/D 10. appeared first on topgradeassignments.org.To answer questions 2, 3 and 6, optical rotation of ( 1 R ,2 R )-()-1,2-Diaminocyclohexane []20/D 10. was first posted on October 16, 2020 at 6:39 pm.©2019 “topgradeassignments.org”. Use of this feed is for personal non-commercial use only. If you are not reading this article in your feed reader, then the site is guilty of copyright infringement. Please contact me at admin@topgradeassignments.org “Is this question part of your assignment? We Can Help!”
Columbia Southern University Unit 5 The Impacts of Technology on Communication Journal
Question Description I’m working on a other report and need a sample draft to help me learn. Technology has changed almost every part of our