Please provide a hand drawn picture of the LUMO for camphor
HUWUver. If you have difficulty using this software, you may provide hand-written answer, take a picture and upload them in the assignment. at is recommended to use CAMSCANNER app on your phone to complete the task. Question 1 4 pts 1) Draw (ChemSketch or hand-drawn) and name all the possible carboxylic acid and ester isomers with C3H2O2 molecular formula. 2) Show the esterification reaction of the two compounds that produce one of the esters. Upload Choose a File <Back Chapter...
Question 1 4 pts Use ChemSketch or ChemDraw software (or hand drawn) to provide condensed and line-angle structures of the following organic compounds. a) methyl propanoate b) 2,4-dibromopentanoic acid Upload Choose a File
Reduction of Camphor Lab 1) Provide a mechanism that accounts for the formation of both Borneol and Isoborneol. 2) In lecture we have consistently discussed the fact when we add to a sp^2 hybridized carbon we normally see no facial preference. Use your mechanism to explain why more isoborneol is formed from the reduction reaction. How would you expect the product distribution to change if methyl groups are missing from the camphor structure.
explain please
(*)-Camphor has a specific rotation of +44 degree. If you have a mixture of 34% (+)-camphor and 66% (-)-camphor, what will be the observed rotation of this mixture? Assume 1 g dissolved in 1 mL; the sample cell is 1 dm long. Express your answer in a whole number. The units are provided.
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO molecular formula 2 Based on your textbook, show the vidation reaction of each isomer. If there is no reaction, type R . for the following compounds 1. Provide molecular formula 2. Provide IUPAC 3. Show addition of hydrogen reaction draw structures of the products and provide IUPAC name for the products O a 0 1) Draw (ChemSketch or hand-drawn) and name all the possible...
When awsering please provide a picture from logix pro
software. PLEASE BE DETAILED AND NEAT.
2.
please help
14. Using FMO theory, determine whether the cycloaddition drawn is symmetry-allowed or symmetry forbidden. Show all work including molecular orbital interactions. Hint: Draw the LUMO of the allylic cabocation and the HOMO of 1,3-butadiene. + (CH₂ Н.С -CH₂
Please provide a mechanism that includes
the formation of both products.
Why is isoborneol formed more in the reduction reaction? How
would product distribution change if methyl groups were missing
from camphor?
NaBH4 MeOH -OH OH Borneol Camphor Isoborneol
please find the integration and tell what each peak
represent
H3C CH3 CH3 camphor
please help
PART D 13. Using FMO theory, determine whether the cycloaddition drawn is symmetry-allowed or symmetry forbidden. Show all work including molecular orbital interactions. Hint: Draw the LUMO of me any carbocation and the HOMO of ethylene. CH2H2C 112 + - 1 + CH₂ H₂C