Give a detailed mechanism for conversion of 2,7-dimethyl-2,6-octadiene, using H3PO4, into 1,1-dimethyl-2-isopropenylcyclopentane.
Give a detailed mechanism for the reaction that occurs when ethyl methylmalonate CH3-CH(C=OOC2H5)2, acetone and 2-chloroacrylonitrile (CH2=CClCN) react in the presence of a base, to yield an epoxy compound CH3-C(EtOOC)2-CH2-C(NC)-O-C(CH3)2
Give a detailed mechanism for the reaction of o-fluorobenzophenone (Ar-C-(=O)-Ar-F)....Ar=benzene ring... with amide ion (NH2/NH3) to yield H2N-C(=O)-Ar + Ar-F
For OTA 104318 This is a synthesis problem. I have four starting materials and their corresponding products. I need all the mechanisms and reagents.
FOR OTA 104318 I need help determining the absolute stereochemistry of three molecules and an explanation as to why it is so.
stability and (R or S) configuration OTA#104318
This is a very simple problem. I chose and explain which one of the chair conformations is more stable. Then I need assign (R or S) configuration to two molecules and determine if they are optically active.
major organic products for reactions OTA#104318
Need the major organic products of a few reactions. Stereochemistry is needed.
Reaction of styrene heated w/ (aq)sulfuric acid THIS PROBLEM IS FOR OTA 104318 ONLY
See attached file for question and related mechanisms
What is aspirin's heat of formation?
Hi, What is aspirin's heat of formation? Thank you
MS spectrum and NMR spectra; THIS PROBLEM IS FOR OTA 104318 ONLY
Please see attached files 1 and 2