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
What products would you expect from reaction of 1-methylcyclohexene, 2-methylpropene, 3-hexene with the following reagents? (draw...
5. What kind of monomer should be used to synthesize the following polymer: OCH3 CH3 CH3 +CH2-CH-CH2-CH-CH2-CH+ çı ç ç ç ç çı +CH-CH-CH-CH-CH-CH+ 6. What products would you expect from reaction of 1-methylcyclohexene, 2-methylpropene, 3-hexene with the following reagents? 1) aqueous acidic KMnO4 2) 03, followed by Zn, CH3CO2H
3. Draw the stereoisomeric structure of the products that you would expect from the bromination of the following Compounds using Br2 in CCl4. Use sawhorse projections. A. cis-3-hexene B. trans-3-hexene
draw structures for the following compounds 1. 3-hexene 2. 2-pentyne 3. trans-3-hexene 4. cyclobutane 5. 3-ethyl-1-methylcyclohexene
Give the structure of the products you would expect from the reaction (if any) of 2-butyne with Li/liquid NH3. If there is no product, simply draw the reactant, 2-butyne Give the structure of the products you would expect from the reaction (if any) of 2-butyne with O3, then HOAc. If there is no product, simply draw the reactant, 2-butyne. How many equivalents of product will be created for one equivalent reactant?
chapter 9, a,b,c 3) a,b,c 9-31: a,b,c,d c) Chapter 9 1) What products would you expect from the following reactions? a) b) CCH1 HBr- ? c) 2) Arrange the carbocations below in order of increasing stability. Determine primary, se 3) Draw structures corresponding to the following names: a) 5-tert-Butyl-2-methyl-3-octyne b) 3,5-Heptadien-1-yne c) (E)2,2,5,5-Tetramethyl-3-hexene 9-31. Predict the products from reaction of 1-hexyne with the following reagents a. 1 equivalent HBr b. 1 equivalent C12 c. H2, Lindlar catalyst d. 2 equivalent...
B only please 6| What products would you expect to obtain from reaction of 1-methylcyclohexanol with the following reagents? a) HBO b) Na2Cr2O7 (oxidizing agents)
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.
Draw the organic product(s) you would expect from the following reaction. Assume products derive from the most stable carbocation intermediate(s). Draw the organic product(s) you would expect from the following reaction. Assume products derive from the most stable carbocation intermediate(s) + HCl (1 mole) → You do not have to consider stereochemistry. If there is more than one major product possible, draw all of them. Draw one structure per sketcher. Add additional sketchers using the dropdown menu in the bottom...
Help me please as soon as possible i need the solutions for those questions s, show structures of reac the products for both reactions. a) What is/are the product(s) of the treatment of 3-methyl-1-butene with aqueous acidic What is/are the product(s) of the treatment of 2-methyl-2-butene with aqueous basic KMnO4? b) 36) (3 pts each) Predict the products (name and structure) from reaction of 3-hexyne with the following reagents: a) H2, Lindlar catalyst b) Li in NH3 c) HgSO4, H2SO4...