1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and...
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...
Worksheet-CH 8 and 9 SN1 and SN2 Reactions 1. For the following Alkyl halide indicate which position will react under SN1 reaction U
2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3CCI CH,OH CH,CH
The following alkyl bromide can react with NaF via an Sn1 mechanism. Draw the mechanism and product(s) of this reaction. Be sure to pay attention to stereochemistry, if applicable.
Which alkyl halide in each of the following reactions will react faster in an SN2 reaction with hydroxide (-OH)? Explain. Hint, some of these compounds are unreactive in SN2 reactions- be sure to think about what type of alkyl halide undergoes SN2 reactions! Bromobenzene or benzyl bromide CH3Cl or (CH3)3Cl CH3CH=CHBr or H2C=CHCH2Br
Which alkyl halide shown below would react the fastest under typical SN2 conditions?
Which of the following alkyl halide will not undergo SN1 or SN2 reaction? PA
7. Draw the structure of the products of the following reactions. Indicate whether they will react under Syl conditions, or Sn2 conditions. If there is no reaction, write "NR”. Indicate stereochemistry where appropriate Меон CH,OH OH CHỊCHO HO
2. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (primary, secondary, or tertiary alkyl halide), nucleophile (strong or poor), and the solvent type (protic or aptrotic). Specify the type of reaction mechanism (SN1 or SN2), show the curved arrow mechanism and draw the products as 3D structures to illustrate stereochemistry. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (1º, 2º, or 3 alkyl halide). mucleophile (strong or poor),...
_1. An alkyl halide which might be expected to undergo rearrangement under Snl or E1 conditions is: HZC Br CH3 A. 1 B. | F—CH,BH C. CH3-C-CH-CH, CHz CH3 D. CH3 CH3-C-CH2CH2-Br CH3 E. A Br 2. Your task is to convert 2-chloropentane into 1-pentene. Which reagents would you choose? a) NaOH/H20 b) KOH/CH3OH c) CH3ONa/CH3OH d) CH3CH2ONa/CH3CH2OH e) (CH3)3COK/(CH3)3COH 3. Circle the reaction below which is faster in polar protic solvents. OH,H,O A. CH,CH,CH,Br- CH,CH,CH,OH + Br or SH.RSH...