explain why a polar protic solvent speeds the rate of an SN1 mechanism
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explain why a polar protic solvent speeds the rate of an SN1 mechanism
Write the mechanism of the following substitution reaction Explain why Polar protic solvents favor SN1 reactions. Do you expect this substrate to react under SN1. explain your answer.
1. why does benzyl bromide react under both Sn1 conditions and Sn2 conditions? 2. To promote the Sn1 mechanism we used AgNO3 in a polar, protic solvent. True or False? Why?
Compound B, tert-butanol, is a polar, protic molecule that can
be used as a solvent for E1 reactions. True or False. Explain.
2. True or False Compound B, tert-butanol, is a polar, protic molecule that can be used as a solvent for E1 reactions. used for Ez H ou HC CH3 3. True or False Chloromethane and sodium acetate react to produce methyl acetate by an Sn1 mechanism. OH H + NaCl H HCONa OH CI H I fastest slower...
Explain the effect of the solvent on the reaction kinetics with respect to an SN1 mechanism? - solvent used was 60/40 acetone/water solution up to 100ml
a. Label each of the following as a nonpolar, borderline polar, or polar solvent. b. Label each solvent as protic or aprotic c. Then, label which reaction the solvent will help promote: SN1, SN2 or neither. HO CI CI dichloromethane moi propanol acetone benzene
please explain!!
3 e) Which solvent is a polar protic solvent? a) ether c) ethanol b) dimethylformamide d) hexane Circle the correct name for the molecule shown below. Br (trans)-3-bromo-4-methyl-4-heptene (E3-bromo-4-methyl-3-heptene (Z)3-bromo-4-methyl-3-heptene (cis)-3-bromo-4-methyl-3-heptene g) Circle the reaction that would have the fastest rate. NaSH DMF SH NaOH OH B DMF NaSH DMF Br SH NaOH Br он DMF h) Circle the strongest nucleophile in methanol (CH,OH) F Br
1-Butanol reaction with sodium bromide and sulfuric acid. Draw the reaction mechanism. Explain why the reaction would prefer a polar protic solvent.
why Sn2 reactions will not work with polar protic solvents? draw structures to explain if possible please
Explain the effect of the solvent on the reaction kinetics with respect to an SN1 mechanism. How to explain 50%/50% acetone/water & 60%/40% acetone/water with reference to the above to the above (from results half life was way less in 50/50) According to the data chart, the Rate constant for the hydrolysis of tertbutylchloride in 50/50 acetone/water (volume) is: k=1.03E-2/min^1 The rate constant for the hydrolysis of tertbutylchloride in 60/40 acetone/water is: K=2.9E-3/min^-1
HWS 5: Due 10/30/2019 15 points total SN1, SN2, Elimination pt 1 1. (10 pts) For the following reactions: a. Label the Nucleophile (Nu) and whether it is strong or weak b. Label the Electrophile (E) and whether it is primary, secondary, or tertiary and circle the leaving group C. Label the Solvent and whether it is polar protic or polar aprotic d. Categorize each as preferring SN1, Preferring SN2, or could do either e. Draw the product of the...