Suggest a likely structure for C6H6 if it produces 4-methyl-2pentanone?
Name the reagents of this reaction and draw the mechanism for the reaction
Suggest a likely structure for C6H6 if it produces 4-methyl-2pentanone? Name the reagents of this reaction and draw the mechanism for the reaction
Draw Questions the structure for (42,6E) - 3-chloro-5-ethyl-4-methyl-4,6- undecadiene. What is the lupAl name for the following compounds. Provide a mechanism for the reaction below.
Be sure to answer all parts. Draw the structure of 4-methyl-2-heptanol. Then draw and name the product that you would expect to produce by its oxidation. Part 1: Structure of 4-methyl-2-heptanol: view structure Part 2: Structure of oxidation product: no structure shown Part 3: Name of product: 4-Methy-3-heptanal 4-Methylheptanone 4-Methyl-3-heptanone 4-Methyl-2-heptanone
Draw the structure for 3-isobutyl-4-methylhexane. What is the correct IUPAC name for this structure? a. 3-methyl-4-isobutylhexane b. 2,3-diethyl-5-methylhexane c. 4-ethyl-2,5-dimethylheptane d. 2-methyl-4-isobutylhexane e. 1,1-dimethyl-3-ethylhexane
Hydration of a 3 carbon alkyne with certain reagents produces CH_3-CH=CH-OH a. What is the name given to that type of compound? b. The product shown above is not the product actually isolated in this reaction. It converts to another compound in the basic solution. Draw the structure of the molecule it converts to and, using curved electron movement arrows, show all the steps in the mechanism of the conversion. c. The transformation you wrote out as a mechanism in...
Show the mechanism of the reaction shown below (include the structure of the reactive intermediate and the addition product formed during the initial addition step): Name the following (use E, Z or cis/trans as needed): d) Draw the structure of Z-2-methoxy-4-methyl-3-hexene
Draw the skeletal structure of the following compounds a. 3-ethyl-4-methyl-1,5-heptadiene b. 2,3-diethyl-3-methyl-1,4-pentadiene Determine the products of the following reactions. Also demonstrate the mechanism in each reaction
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all resonance structures for each possible substitution position to explain why methyl m-nitrobenzoate was the favored isomer.
please draw a step-wise mechanism for the reacrion between 1-iodo-4-nitrobenze and 2-methyl-3-butyn-2-ol with the reagents Pd(PPh3)2Cl2 , Cul, Et3N.
1. Suggest a reasonable mechanism for the following reaction mage. i.EtON, EtOH, 25°C ii. Hz0 Answer: 2. There are several possible cyclization products that might be formed when 5-methyl-6-oxoheptanal undergoes intramolecular aldol condensation in presence of ethoxide. Draw the structures of all these possible products. Comment on which of these is likely to be the major product, clearly explaining your rationale. Answer:
Write any e2 reaction. Identify structures for the reagents and products, and the mechanism of the reaction. What is the rate law for the e2 reaction? Draw a structure for the transition state.