Draw the mechanism to show how you would accomplish the synthetic conversion of 1-methylcyclohexene to 1-bromo-1-methylcyclohexane....
Show how you would accomplish the following synthetic conversion
starting with ethanol as the only source of organic carbon
atoms. You may use any necessary inorganic reagent and
solvent. Show all reaction steps, reagents and conditions used.
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent....
(10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
Show how you would accomplish the following conversion. More
than one step is likely necessary.
Thankyou!!
Extra Credit Show how you would accomplish the following conversion. More than one step is likely necessary. CH3 CH3
4. Why does the reaction of trans-1-bromo-2-methylcyclohexane yield the non-Zaitsev elimination product 3-methylcyclohexene on treatment with a base? Draw structures in chair conformations to support your explanation. сн, сн, КОН Br
HELP
Other Nether What is the TUPAC name of the following compound? -CH3 a) 3-Bromo-2-methylcyclohexene 2-Bromo-1-methylcyclohexene b) 1-Bromo-2-methyl-2-cyclohexene d) 6-Bromo-1-methylcyclohexene 9. Carbon-carbon double bonds do not freely rotate like carbon-carbon single bonds. Why? a) The double bond is much stronger and thus more difficult to rotate b) Overlap of the two 2p orbitals of the pi bond would be lost c) The shorter bond length makes it difficult for the attached groups to rotate past each other. d) Overlap of...
Extra Credit Show how you would accomplish the following conversion. More than one step is likely necessary. CH3 CH3
What is the mechanism of the Reaction of (1S,3R)-1-bromo-3-methylcyclohexane with cyanide?
Write the structural formula for 1?bromo?6?methylcyclohexene. draw structure ...
Question 6 - 10 pts. Homework • Unanswered When (cis)-1-bromo-2-methylcyclohexane is treated with methanol and heat, four different products are formed -- two by substitution (1-methoxy-2- methylcyclohexane and 1-methoxy-1-methylcyclohexane) and two by elimination (1-methylcyclohexene and methylidene cyclohexane (you will have to look that one up!)). What conditions could be used to change the outcome of this reaction by promoting the production of 3-methylcyclohexene as the product? [] Fulls
I am a beginner in organic chemistry. Please help
A graduate student wanted to make methylenecyclobutane using the following reaction. Propose a structure for the major product and give a mechanism to account for its formation (5 pts). H SO -CH,OH - major product heat minor product (BONUS)Show how you would accomplish the following synthetic conversion. This is a synthesis problem. Please show the steps required and each compound formed along the way NO MECHANISM NECESSARY. (3 pts) 2-methylcyclohexanol 1-bromo-1-methylcyclohexane