B only please 6| What products would you expect to obtain from reaction of 1-methylcyclohexanol with...
help please 6) What products would you expect to obtain from reaction of T-methylcyclohexanol with the following reagents? 4) HIBI b) Na Cro oxidizing agents) How would you prepare the following ether using a Williamson synthesis?
please show the reaction mechanism to obtain all of these products from 2-methylcyclohexanol OA као Н3РО4 см3 zo alcohol
Draw a structure for the major organic product you would expect from reaction of 1-methylcyclohexanol with H2SO4. Must be drawn
Draw the organic products you would expect to obtain from reaction of the following model triglyceride with excess Br2 in CH2Cl2.
What products would you expect from reaction of 1-methylcyclohexene, 2-methylpropene, 3-hexene with the following reagents? (draw it out) a) aqueous acidic KMnO4 b) O3, followed by Zn, CH3CO2H
(i) Carvone is the major constituent of spearmint oil. What products would you expect from the reaction of carvone with the following reagents? Carvone CH3MrBr, then H30* (a) LIAIH4, then H30* (b) (c) H2, Pd (d) НОСН,СH2ОН, НСІ (е) CH;NH2 (i) Carvone is the major constituent of spearmint oil. What products would you expect from the reaction of carvone with the following reagents? Carvone CH3MrBr, then H30* (a) LIAIH4, then H30* (b) (c) H2, Pd (d) НОСН,СH2ОН, НСІ (е) CH;NH2
please explain not just answers thanks 13. What products would you expect from the reaction between (S)-2-iodobutane and each of the following nucleophiles: a) NaSH b) NaSET c) NaCN
Give the structures of the major organic products you would expect from reaction of m-toluidine (m-methylaniline) with the following reagents: (a) Br2 (1 equivalent) (b) CH3I (excess) (c) CH3COCl in pyridine (d) The product of (c) then HSO3Cl
How many products would you expect from the reaction of (S)-2-methylcyclohexanone with methyl magnesium bromide (include the stereoisomers)? Draw the stereoisomers of the product and specify the relationship between them. Following is a cyclic acetal formed from cyclohexanone. What are the reagents required for this reaction? Also write a stepwise mechanism for the formation of this acetal from cyclohexanone. Show how to synthesize the following compounds using a Wittig reaction. Design the synthesis of compound A (5-(1-hydroxycyclohexyl)pentan-2-one) starting from cyclohexanone...
what products would you expect from the following reaction? (alkene organic reaction with NBS/ CCl4) What product(s) would you expect from the following reaction? You do not have to consider stereochemistry. If more than one structure fits the description, draw them all. Draw one structure per sketcher. Add additional sketchers using the dropdown Separate structures with + signs from the dropdown menu.