(a) Draw the stuctures of the products that would form as a result of each of the reaction mechanisms shown. (b) Label the nucleophile (Nu-) and the electrophile (E+) in each reaction.
(a) Draw the stuctures of the products that would form as a result of each of...
(B) In the boxes below, draw the two self-condensation pro products that result from the mixture in Model 2. Use the roles reagent listed in each box to determine the products. Eation products and two mixed condensation Use the roles (Nu, Ee) for each Self Condensation Nuo = A ΕΦ = A Self Condensation Nuo = B E =B Mixed Condensation NuO = A E = B Mixed Condensation NuO = B ΕΦ = A 5. Mixed condensations can also...
Draw the mechanisms arrows that would show how the product is
formed in each elementary step. Make sure to draw the products of
the reaction and name the elementary reaction step(proton transfer,
sn2, coordination, heterolysis, e2, nucleophilic addition,
carbocation rearrangement, nucleophile elimination, electrophilic
addition, electrophile elimination).
4. (6pts) Label each molecule as a nucleophile or electrophile AND draw an arrow pointing to the atom on the molecule that would be the nucleophile or electrophile CI CEN HTΉ I verbo on si smith H-C-OH I-O-I H₃C – NH₂ Hool H3CH
1. Either draw the product that the arrows predict or provide arrows that account for the product drawn. Each is a nucleophile/electrophile reaction. Label each starting material as either Nu: or E+. 3 pts ea eo ное на-ві H₂C-00 H₂Coro
What is the effect of the first step in the acid-catalyzed reaction mechanism shown? Select all responses that apply. General mechanism: Acidic conditions - H-A -H + :A® R Y LG * H-Nu - LG - H Nu RDS öHAO ÖH a ñ =Rt LG / Corant) Nu Rtió + MÃ . solvent) u® H ÖH op + 1 nocor OH H-LG e s Stre-H + ÄⓇ = RP R ALG o -H+A - R . Nu it solvent) H-LG...
complete the following reaction mechanisms by drawing the
correct product or intermediate formed in each reaction. on the
side of the reactants, label the nucleophile and the electrophile
(front)
show using electron-pushinh arrows how the anion shown is
converted to two other resonance structures (back)
Complete the Following Reaction Mechanisms by drawing the correcting product or intermediate formed in each reaction. On the side of the reactants, label the nucleophile and electrophile. (4 points each) Ci Me H Ме Me...
4. (4 pts) Label the nucleophile and electrophile and draw the products of the following Si2 reaction. Be sure to indicate the appropriate stereochemistry. acetone N3 (2 pts) Would the reaction above be faster or slower if each of the following substrates were used instead of trans-1-iodo-4-methylcyclohexane? 5. a. iodoethane FASTER SLOWER b. trans-1-chloro-4-methylcyclohexane FASTER SLOWER
Additional Questions: 15. (a) An alcohol (pka = 15) is reacted with NaNH, (pka = 36). What role does the alcohol play (acid, base, no role)? (b) Draw the reaction of ROH and NaNH2. Use curved arrows to show electron movement R-O-H + O NHA Na slavonotons boi gelts, Part A define NaNH2 as acting as a base and not as a nucleophile? Why do we define 185 or product of the following reaction. What role does the alcohol play?...
Kritik Assignment 5 Chem 267 1) A. Draw the mechanism that produces the major and minor products Make sure you add all arrows!!! And watch out for charges on atoms. B. For any step that involves an acid/base or nucleophile/electrophile reaction label the acid/base or nucleophile/electrophile pairs. C. Label the elimination step (E1cb). NaOH/H30 major and minor heat 2) A. Draw the mechanism for the following Claisen Condensation reaction. B. For any step that involves an acid/base or nucleophile/electrophile reaction...
12. Which is the major product of the reaction shown? (a) (b)
(c) (d) 13. What are all of the possible products formed in the
following reaction? (choose all correct answers) (a) (b) (c) (d)
(e) (f) 14. The three compounds below can form a carbocation in the
presence of H2O and H2SO4. Which ones will form the same
carbocation? (a) I and II (b) I and III (c) II and III (d) all
three will form the same carbocation...