Determine the reagents required to convert cyclohexanone to the following products. C0
5. Identify the reagents you would use to convert cyclohexanone into each of the following compounds NOZ 6. Draw a plausible mechanism for the following transformation:
[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone to the following compound: CH2CH2CO2H Use the minimum number of steps: from one to five are required. List reagents by letter in the order that they are used; example: fa. Reagents Available a. BH3, THF; followed by H2O2, OH g. Nat -CH(CO2C2H5) (from CH2(CO2C2H5)2 + Nat -OC2H5) b. Br2, CH3CO2H h. PBr3 c. HCN, KCN i. PhCH Br d. H307, heat j. Ph3P+- CH2...
provide missing reagents and solvents that is needed to
convert alkene to corresponding products
Provide the missing information (reagents, solvent, etc.) that is necessary to convert the alkene in the box to the corresponding products. OH Noh
only evens
ence of reactions required to convert benzene to the compounds shown. CH b. a. CH2CH CO2H 1036 Determine the sequence of reactions required to convert benzene to the compounds shown. NO2 Cl CH3CH2CH2 10.37 Provide reagents represented as a-c in the scheme. Cl Cl 10.38 Provide reagents repres ented as a-c in the scheme. i c H2N We were unable to transcribe this image
ence of reactions required to convert benzene to the compounds shown. CH b. a....
Synthesize the following compound from cyclohexanone and organic halides having ≤ 4 C's. You may use any other inorganic reagents. Draw all reaction intermediates, and select the single best set of reagents for each of the four reaction steps. Cyclohexanone
Convert 2-butanol to alcohol
Using reactions covered by your text, give the reagents and intermediate products that could be used to convert 2-butanol to alcohol A. 2-Butanol is the only organic compound that may be used. (Hint: The first steps involve conversion of 2-butanol into two different products to be used in a Grignard sequence..)
Predict the products or write the required reagents for the following transformations. Show stereochemistry in the products if pertinent. 4. 1. CH3MgBr 2. Hyo b. OH 1. NaBH4, EtOH HO 2. H3o d. Br 1. Mg, ether 2. НО'Y 3. H
mechanism
and 9) Provide the sequence of synthetic steps necessary to convert cyclohexanone into the compound shown CO2Et ise mechanism for the transformation shown below
From the table of available reagents, select the one(s) you would use to convert toluene (shown above) to each of the following products: (Use the minimum number of steps; in no ease arc more than six steps necessary. List reagents by letter in the order that they are used (example: fa). If an acid workup is required, for example after a Grignard reaction, it must be specified.)
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...