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For each equation state the major reaction pathway that it will undergo. O Hold and drag to reorder a) E1 b) = SN2 c) E2 d) = E2 e) = SN1 f) SN2 = SN1 E1 Br OH a) NaOH d) H2SO4 Br OH b) NaSH e) H2SO4 NaBr Br OTs c) H20 f) NaOH II II

For each equation state the major reaction pathway that it will undergo. O Hold and drag to reorder a) E1 b) = SN2 c) E2 d) = E2 e) = SN1 f) SN2 = SN1 E1 Br OH a) NaOH d) H2SO4 Br OH b) NaSH e) H2SO4 NaBr Br OTs c) H20 f) NaOH II II

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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**Educational Content on Major Reaction Pathways** --- **Instructions:** For each equation below, state the major reaction pathway that it will undergo. Use the provided diagrams to determine if the reaction follows an S_N1, S_N2, E1, or E2 mechanism. --- ### Equations and Pathways a) **Pathway:** E1 ``` Diagram Description: - Reactants: A brominated alkane (2-bromobutane) reacts with sodium hydroxide (NaOH). - Major Reaction Pathway: E1 (Elimination Unimolecular) - Representation: Br-CH2-CH-CH3-CH3 (with NaOH) --> Alkene (E1 product) ``` b) **Pathway:** S_N2 ``` Diagram Description: - Reactants: A brominated alkane (2-bromobutane) reacts with sodium hydrosulfide (NaSH). - Major Reaction Pathway: S_N2 (Substitution Nucleophilic Bimolecular) - Representation: Br-CH2-CH-CH3-CH3 (with NaSH) --> alkane with SH group (S_N2 product) ``` c) **Pathway:** E2 ``` Diagram Description: - Reactants: A brominated alkane (1-bromo-2-methylpropane) reacts with water (H2O). - Major Reaction Pathway: E2 (Elimination Bimolecular) - Representation: Br-CH2-CH-CH2-CH3 (with H2O) --> Alkene (E2 product) ``` d) **Pathway:** E2 ``` Diagram Description: - Reactants: A brominated cyclopentane reacts with sulfuric acid (H2SO4). - Major Reaction Pathway: E2 (Elimination Bimolecular) - Representation: OH-CH2-CH2-CH2-CH2-CH2 (reacting with H2SO4 and producing alkene via E2 mechanism) ``` e) **Pathway:** S_N1 ``` Diagram Description: - Reactants: Cyclohexanol reacts with sulfuric acid (H2SO4) and forms cyclohexyl bromide (via NaBr). - Major Reaction Pathway: S_N1 (Substitution Nucleophilic Unimolecular) - Representation: OH-CH2-CH2-CH
Transcribed Image Text:**Educational Content on Major Reaction Pathways** --- **Instructions:** For each equation below, state the major reaction pathway that it will undergo. Use the provided diagrams to determine if the reaction follows an S_N1, S_N2, E1, or E2 mechanism. --- ### Equations and Pathways a) **Pathway:** E1 ``` Diagram Description: - Reactants: A brominated alkane (2-bromobutane) reacts with sodium hydroxide (NaOH). - Major Reaction Pathway: E1 (Elimination Unimolecular) - Representation: Br-CH2-CH-CH3-CH3 (with NaOH) --> Alkene (E1 product) ``` b) **Pathway:** S_N2 ``` Diagram Description: - Reactants: A brominated alkane (2-bromobutane) reacts with sodium hydrosulfide (NaSH). - Major Reaction Pathway: S_N2 (Substitution Nucleophilic Bimolecular) - Representation: Br-CH2-CH-CH3-CH3 (with NaSH) --> alkane with SH group (S_N2 product) ``` c) **Pathway:** E2 ``` Diagram Description: - Reactants: A brominated alkane (1-bromo-2-methylpropane) reacts with water (H2O). - Major Reaction Pathway: E2 (Elimination Bimolecular) - Representation: Br-CH2-CH-CH2-CH3 (with H2O) --> Alkene (E2 product) ``` d) **Pathway:** E2 ``` Diagram Description: - Reactants: A brominated cyclopentane reacts with sulfuric acid (H2SO4). - Major Reaction Pathway: E2 (Elimination Bimolecular) - Representation: OH-CH2-CH2-CH2-CH2-CH2 (reacting with H2SO4 and producing alkene via E2 mechanism) ``` e) **Pathway:** S_N1 ``` Diagram Description: - Reactants: Cyclohexanol reacts with sulfuric acid (H2SO4) and forms cyclohexyl bromide (via NaBr). - Major Reaction Pathway: S_N1 (Substitution Nucleophilic Unimolecular) - Representation: OH-CH2-CH2-CH
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