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Br NasH. CH, CH3 CH tatok CH, CH, Br

Br NasH. CH, CH3 CH tatok CH, CH, Br

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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Provide the Major product for the following reactions

The image displays two chemical reactions involving alkyl halides. 1. **Reaction 1:** - **Reactant:** The top structure is a brominated cycloalkane with a linear side chain. The cycloalkane is a hexagon, and on its side chain, a bromine (Br) atom is bonded to a carbon atom, with a methyl group (CH₃) attached to the neighboring carbon. - **Reagent:** NaSH (sodium hydrosulfide). - **Arrow:** Indicates the direction of the chemical reaction. 2. **Reaction 2:** - **Reactant:** The bottom structure is a brominated alkane. It consists of a cyclohexane with a four-carbon linear extension, where each carbon atom, except for the brominated ones, is substituted with a methyl group (CH₃). Two bromine (Br) atoms are located on adjacent carbon atoms at the end of the chain. - **Reagent:** t-BuOK (potassium tert-butoxide). - **Arrow:** Indicates the direction of the chemical reaction. These reactions are typically involved in organic chemistry to demonstrate mechanisms such as substitution and elimination.
Transcribed Image Text:The image displays two chemical reactions involving alkyl halides. 1. **Reaction 1:** - **Reactant:** The top structure is a brominated cycloalkane with a linear side chain. The cycloalkane is a hexagon, and on its side chain, a bromine (Br) atom is bonded to a carbon atom, with a methyl group (CH₃) attached to the neighboring carbon. - **Reagent:** NaSH (sodium hydrosulfide). - **Arrow:** Indicates the direction of the chemical reaction. 2. **Reaction 2:** - **Reactant:** The bottom structure is a brominated alkane. It consists of a cyclohexane with a four-carbon linear extension, where each carbon atom, except for the brominated ones, is substituted with a methyl group (CH₃). Two bromine (Br) atoms are located on adjacent carbon atoms at the end of the chain. - **Reagent:** t-BuOK (potassium tert-butoxide). - **Arrow:** Indicates the direction of the chemical reaction. These reactions are typically involved in organic chemistry to demonstrate mechanisms such as substitution and elimination.
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