(9) SN2 Reactions- Predicting Reaction Products. Complete the reactions shown below by drawing the structure of the substitution product. It is not necessary to balance the equations. Draw the proper product stereochemistry, if relevant (inversion of configuration for SN2). acetone (a) NaCI DMF NaOH (b) acetone (c) NaCN

(9) SN2 Reactions- Predicting Reaction Products. Complete the reactions shown below by drawing the structure of the substitution product. It is not necessary to balance the equations. Draw the proper product stereochemistry, if relevant (inversion of configuration for SN2). acetone (a) NaCI DMF NaOH (b) acetone (c) NaCN

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Provide a 3-5 step synthetic route the target molecule from starting material A. Be sure to account for relative stereochemistry and suggest reagents/conditions for each step.
Complete the following reaction scheme. Give all product(s) and indicate major or minor and any relevant stereochemistry (G) H2 CH2 H2 -CH2 Pd/C CH H2C (k) OH ....OH OsO, NMO OH (1) BI2
Provide the structure of the major organic product of the following reaction and? explain the stereochemistry which results in this product. 2-Pentanol reacting with 1.) PBr3, pyridine 2.) NaCN
3. For each of the following reactions, fill in the missing products, reactants, or reagents as appropriate. Account for stereochemistry when appropriate. CI Br KCN CH3OH Ph CH3OH (а) (b) CH3 CH3 KO'Bu 'BUOH Br
Provide the structures of the missing substrates or products for each of the 8) following reactions. Show all relevant stereochemistry clearly on the structures. Note carefully the direction of each reaction arrow! NANH2 NaCN DMF, rt THF b) 1) O, CH,Clz, -78 °C 1. OsO, THF 2. H,S 2) Zn, CH;COOH Br2, light Br2 он conc. H,SO4 MCPBA heat CH,Cl2 1) ВН,- THF NaH 2) H,O2, OH THF 1) NaH Na, NH,() H3C-CEC-CH3 2) CH3I -30 °C 7
Draw the major organic product(s) for the following. - You may assume each reaction occurs just one time. - Show or depict any relevant stereochemistry in the products [R/S or E/Z labels are not needed].
Provide a 3-5 step synthetic route the target molecule from starting material A. Be sure to account for relative stereochemistry and to suggest reagents/conditions for each step CN .CI H3C CN Target molecule starting material (A)