Draw a detailed mechanism for each of the following reactions, including an indication of any proton transfer that takes place.
Draw a detailed mechanism for each of the following reactions, including an indication of any proton...
Draw the complete detailed mechanism (including curved arrows) for each of the following reactions occurring via (A) an SN2 mechanism and (B) an SN1 mechanism. Pay attention to stereochemistry Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions occurring via (a) an SN2 mechanism and (b) an SN1 mechanism. Pay attention to stereochemistry Br + NaOH → NaOH > H3C
8.43 Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions occurring via (a) an S, 2 mechanism and (b) an Swi mechanism. Pay attention to stereochemistry * or Nuct —>?." o Br + NaOH - ? + NaOH - ? н,с fiv) + NaOH ? = > + KBr сн. '+NaOCH, —
Write a detailed mechanism for the reaction shown above which proceeds in six steps including proton transfer steps. Then draw curved arrows that depict electron reorganization for the mechanism step below.
Alkylation and halogenation of alpha carbons detailed mechanism 10.41 Draw the complete, detailed mechanism for each of the following reactions and Braho Be HO ? HO 558 CHAPTER 10 Nucleophilic Substitution and Elimination Reactions 2
Be sure to answer all parts. Draw a stepwise mechanism for the following reaction. OH OH H.C=0 HN N mida Draw the product of each step. :0 Il HN H2CO. draw structure ... proton transfer draw structure proton source proton source draw structure ... +H2O draw structure... draw structure...
A)For each of the following proton transfer reactions (a) draw the products, (b) estimate the pKa’s of the acid and conjugate acid. (Use the functional group to estimate the pKa) B) Circle which side is favored at equilibrium in each of the reactions above (4) (a) For each of the following proton transfer reactions (a) draw the products, (b) estimate the pKas of the acid and conjugate acid. (Use the functional group to estimate the pKa. (12 pts) conjugate acid...
3. (15 points each) Predict the products and present a detailed mechanism for the following reactions. If an intermediate is stabilized by resonance, draw all resonance structures. Show all lone pair electrons and label any charged atoms. Cl2, FeCl;
DROBLEM 20.4 Draw the complete, detailed mechanism and predict the overall for each of the following reactions. 1. NaOH, H0 1. NaOH, H2o 2. HCI DROBLEM 20.4 Draw the complete, detailed mechanism and predict the overall for each of the following reactions. 1. NaOH, H0 1. NaOH, H2o 2. HCI
4) Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like "proton transfer without showing the arrows for that step is not an acceptable answer NOE, EIH
3. Draw the arrow-pushing mechanism of the reaction, including all proton transfer steps. 4. Below is the structure of your product, benzocaine, with protons labelled A-E. The 'H NMR spectrum is provided on the next page. Describe the multiplicity (with J values) and integration you would expect to observe for each of the protons. Which peak would you expect to have a higher chemical shift, C or D? Draw resonance OSO structures of benzocaine to explain your reasoning. NH2E