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1) For the following transformations involving one elementary step each: (i) Draw &+ and 8- on the atoms that are most electron deficient or electron rich on the starting material which will help you to draw the mechanism (ii) provide mechanism arrows to describe electron flow for these transformations (ii) name the elementary steps on blanks (not as important but useful for recognition/categorization) O:CEN -I0 CN a) b) SPh SPh H-O H. d) RMi E limination CH3 O CH3 H- : Required format for multi-step mechanisms. Helps you keep track of where you are heading and saves you having to redraw product! OCH3 OCH3 :0: Bonds Made Bonds Broken e.g. C1-02 C4-H so number your atoms on SM to keep track of what is happening during the reaction (=book keeping); cross out bonds made/ broken as your mechanism demonstrates each step) reagent(s) 1.. SM Product(s) СЗ-04 reaction conditions OCH3 Intermediate #1 Nucleophilic additưon on Carbonyl caeben Int. #4, etc. Int. #2 femoval of Having group (chlopide ian Int. #3

1) For the following transformations involving one elementary step each: (i) Draw &+ and 8- on the atoms that are most electron deficient or electron rich on the starting material which will help you to draw the mechanism (ii) provide mechanism arrows to describe electron flow for these transformations (ii) name the elementary steps on blanks (not as important but useful for recognition/categorization) O:CEN -I0 CN a) b) SPh SPh H-O H. d) RMi E limination CH3 O CH3 H- : Required format for multi-step mechanisms. Helps you keep track of where you are heading and saves you having to redraw product! OCH3 OCH3 :0: Bonds Made Bonds Broken e.g. C1-02 C4-H so number your atoms on SM to keep track of what is happening during the reaction (=book keeping); cross out bonds made/ broken as your mechanism demonstrates each step) reagent(s) 1.. SM Product(s) СЗ-04 reaction conditions OCH3 Intermediate #1 Nucleophilic additưon on Carbonyl caeben Int. #4, etc. Int. #2 femoval of Having group (chlopide ian Int. #3

Chemistry
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...
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I need help with part 3 of this problem, naming the elementary step occuring in each. 

1) For the following transformations involving one elementary step each: (i) Draw &+ and 8- on the atoms that are most electron deficient or electron rich on the starting material which will help you to draw the mechanism (ii) provide mechanism arrows to describe electron flow for these transformations (iii) name the elementary steps on blanks (not as important but useful for recognition/categorization) -IO :CEN CN a) b) 學0 :SPh SPh H-O c) d) RHi E limination : CH3 O:0 CH3 H-O : e) f) Required format for multi-step mechanisms. Helps you keep track of where you are heading and saves you having to redraw product! ?OCH3 : OCH3 O: :0: reagent(s) Product(s) Bonds Made Bonds Broken C3-04 SM OCH3 reaction conditions e.g. C1-02 C4-H so number your atoms on SM to keep track of what is happening during the reaction (=book keeping); cross out bonds made/ broken as your mechanism demonstrates each step) Intermediate #1 g) Nucleophi ic additron on carbonyl carban Int. #4, etc. Int. #2 lemoval of Having. group (chlopide ión) Int. #3
Transcribed Image Text:1) For the following transformations involving one elementary step each: (i) Draw &+ and 8- on the atoms that are most electron deficient or electron rich on the starting material which will help you to draw the mechanism (ii) provide mechanism arrows to describe electron flow for these transformations (iii) name the elementary steps on blanks (not as important but useful for recognition/categorization) -IO :CEN CN a) b) 學0 :SPh SPh H-O c) d) RHi E limination : CH3 O:0 CH3 H-O : e) f) Required format for multi-step mechanisms. Helps you keep track of where you are heading and saves you having to redraw product! ?OCH3 : OCH3 O: :0: reagent(s) Product(s) Bonds Made Bonds Broken C3-04 SM OCH3 reaction conditions e.g. C1-02 C4-H so number your atoms on SM to keep track of what is happening during the reaction (=book keeping); cross out bonds made/ broken as your mechanism demonstrates each step) Intermediate #1 g) Nucleophi ic additron on carbonyl carban Int. #4, etc. Int. #2 lemoval of Having. group (chlopide ión) Int. #3
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