please help me 1. Provide the product/s and mechanism for the following reaction. Explain if the...
1. Provide the product/s and mechanism for the following reaction. Explain if the reaction condition favors a SN1 or SN2 mechanism. Determine the stereochemistry configuration (S/R) o the product/s. (25 points) CI NaCN DMSO
1. Provide the product/s and mechanism for the following reaction. Explain if the reaction condition favors a SN1 or SN2 mechanism. Determine the stereochemistry configuration (S/R) o the product/s. (25 points) CI NaCN ♡ DMSO
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms a h a NaCN DMF come NaSH DMSO NaOH DMSO a) M y NaOCHZ Naoch,, H2O NaOCH; HO
because it is 3° carbon shouldnt it be an SN1 reaction? even though it is in a aprotic solvent with a strong Nu? Sodium Cyanide reacts with 2-bromobutane in dimethylsulfoxide to form a substitution product. Identify the configuration of the 2-bromobutane structure shown below. Then draw the substitution product formed when this enantiomer reacts with NaCN in DMSO, and indicate the stereochemistry of the product. O O (R)-2-bromobutane (S)-2-bromobutane Use wedge-and-dash bonds to show stereochemistry, and show explicitly the hydrogen...
3. For each reaction, draw the structure of the major product(s) including stereochemistry where appropriate. Fill n the box below each arrow with the mechanism(s) that will be followed (SN1/E1, SN2, or E2). For SN1/E1 reactions, draw products for both. NaCN DMF tBuOH 言言言 MeOH * | CH30 CH OH DMSO R-2-bromopentane
For each of the following transformations: a) Show all Products formed State whether the mechanism favors SN1 or SN2 b) c) Show stereochemistry (*R/S) where applicable. d) Show an arrow that indicates which side of the reaction is favored, products or reactants. Br acetone + NaCN CH3CH2CH2NH2 ш HСІ он
Provide the mechanism for the following reaction. Determining if the reaction is an SN2, SN1, E2 or E2 reaction will help you make sure you provide the correct mechanism. 2. Provide the mechanism for the following reaction. Determining if the reaction is an SN2, SN1, E2, or E2 reaction will help you make sure you provide the correct mechanism (2 Points). NaOH
Please please help and read the directions, thanks in advance! Chapter 6 Homework Assignment Chem 235/237 -Organic Chemistry 1 Name: Due Date: 10/17/18 Predict the product(s) of the following substitution reactions and provide the mechanism responsible (i.e, SN1 or SN2). 1. NaCN NaOCH3 DMF H20 (CH3)2S DMSO CH3OH CI
4. Predict the products of the following reactions & indicate whether they are most likely to go through an SN2, SN1, E1, or E2 mechanism. NaCN DMSO NaOH CH3OH heat Only one product is formed in the following E2 elimination reaction. Draw an arrow-pushing mechanism for the reaction and provide the correct product structure. Include a 3-D drawing (chair conformation) displaying proper stereochemistry of the transition state to explain formation of only the major product. CH3 •Br NaOCH3 ~"'CHS