Please note that 3-methyl-3-hydroxyacetophenone is an ambiguous name of a compound. I am assuming here our target molecule is 5-methyl-3-hydroxyacetophenone. However, the correct name of the compound is still: 1-(3-hydroxy-5-methylphenyl)ethan-1-one.
start with methylcyclohexane and show synthesis to 3-methyl-3-hydroxyacetophenone
Explain why 3-methylcyclohexene is more stable than
methylcyclohexane.
ОН HA -H20 2-Methylcyclohexanol cis, and trans) 3-Methyl- 1-Methyl Methylene- cyclohexene cyclohexene cyclohexane
4. Newman projection-like view of chair conformation of methylcyclohexane with methyl group in the axial position. 5. Demonstration of steric strain in of axial methyl group in methylcyclohexane. Briefly define “steric strain”.
Write equations and mechanisms in the synthesis of the following compounds. Start with a 3-pentanone and utilize any other reagents needed. More than one step may be necessary. 1) 3-Methyl-3-chloropentane
Two-step Synthesis: formation of methyl 3-nitrobenzoate What happens to the methyl group of 3-nitroacetophenone in the haloform reaction? A) it comes off as chloroform B) nothing C) it comes off as dichloromethane
QUESTION 9 CH3 What is the name of the following compound? H₂C 1-methyl-3-ethylcyclohexane 1-ethyl-3-methylcyclohexane 1-methyl-5-ethylcyclohexane m-methylethylcyclohexane QUESTION 10 A compound is named incorrectly as 2,4-diethylpentane. What would be the correct name of this compound? 5-ethyl-3-methylhexane 3-ethyl-5-methylhexane 3,5-dimethylheptane 2.ethyl-4-ethylpentane Click Save and Submit to save and submit. Click Save All Answers to steal answers BO 7
Propose a reasonable synthetic strategy for the synthesis of trans-6-methyl-3-heptene from 4-methyl-1-pentyne.
4. Write out the synthesis of the end product from the start material and show the reagents for each synthesis step and product. The mechanism is not needed. a. Start material: End material: Br End material: b. Start material: Br N3
Question 24 (1 point) Give the IUPAC name for the following compound: A) 2,4-Diethyl-1-methylcyclohexane B) 2-Ethyl-1-methyl-4-ethylcyclohexane OC) 1,3-Diethyl-4-methylcyclohexane D) 1,5-Diethyl-2-methylcyclohexane E) 1-Methyl-2,4-diethylcyclohexane Previous Page Next Page Page TUTOF 11th Edition
Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. Reactant (2-methyl-2-butene) Reagent 1rightarrow Step 1 Product Reagent 2 rightarrow Step 2 Product Reagent 3 rightarrow Final Product (3-bromo-3- methyl-2- butanol)
10) Show how to synthesize 4-Phenyl-2-butanone using the Acetoacetic Ester Synthesis. Start with Ethyl 3-oxobutanoate (C6H1003).