Which of the following forms a carbocation fastest under Sn1 conditions? Its of off
1. Given the following structures that react by Sn1, which would react fastest and which would react slowest. Give reasoning. 5-bromo-1,3-pentadiene, bromocyclopentane, (R)-2-bromo-2-methylhexane. 2.If bromocyclohexane reacts faster than chlorocyclohexane in an Sn2 reaction, what could be the reason? 3.You wish to substitute the bromine in the following molecules with a nucleophile. Explain whether the given molecule would react by Sn1 or Sn2 mechanism and explain why. 1-methyl-1-bromo-cyclohexane, 1-bromopropane, 2-bromohexane. 4. Why does benzyl bromide react under both Sn1 and Sn2...
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. BEBE 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. HyCc CH OH CH CHE
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...
1.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2 conditions? Draw the structures of each using the bond line method and explain your answers. 1-methyl-1-bromocyclohexane, 1-bromopropane, 2-bromohexane 2.) What is the order of reactivity of the following reagents under SN1 conditions? Under SN2 conditions? Explain your answers. CH3CH=CHBr, CH3CH=CHCH2Br, CH3CH2CH2Br 3.) We did not use crotyl chloride in this experiment. However, based on your knowledge of SN1 and SN2 predict the behavior of...
16.) Which of the following esters reacts fastest under conditions of acid-catalyzed hydrolysis? A) ethyl propanoate B) ethyl acetate C) ethyl 2-methylpropanoate D) ethyl 2,2-dimethylpropanoate
Which alkyl halide shown below would react the fastest under typical SN2 conditions?
Propose a mechanism for the following reaction under conditions that favor a SN1 reaction. HO -OH & Br
6. Propose a mechanism for the following reaction under
conditions that favor a SN1 reaction.
Br HO Σ ΟΗ
Which of the following reacts fastest with methanol by the SN1 mechanism? A) CH3CH2CH2CH2CH,Br B) CH3CH2CH2CHCH: C) (CH3)2CCH2CH Br D) (CH3):CCH Br WBC ma D. QUESTION 19 A) Cce ( CCC 1 (CRC 410 (CHCOM
6. Propose a mechanism for the following reaction under conditions that favor a SN1 reaction. (16 points) HO X ОН Br