man Campus Depa(a) Draw the three products (constitutional isomers) obtained when 2-methyl-3-hexene reacts with water anda trace of H2SO4. Hint: one product forms as the result of a 1,2-hydride shift. (1.5 pts)This is the acid-catalyzed alkene hydration reaction.

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Answered: man Campus Depa (a) Draw the three…

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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5:10 34 7. Draw the structure of the intermediate (including stereochemistry, lone pair(s) and formal charge(s)) that forms when the alkene shown below (cis-3-hexene) reacts with Br₂ in an inert solvent. (4 pts) CH3 -CH3
S 4 Draw all possible isomers for the chemical formula C₂H₂O. Select 2 000 000 → % 5 C Draw H 6 O Rings MacBook Pro & 7 * 8 More ( 9 ) 0
10. Draw a line structure for each organic product of the reaction shown below, including relevant stereochemistry. Do not draw multiple structures of the same compound. (6 pts) SN2 + HBr ???? OH
6. Draw the products of the following reactions. (3.0 pt) NaOH/H2O Η NaOH/H2O дель NaOH/H20 Δ
3. What is the IUPAC name for the following compounds? (2 pts.) a) b) H se H OH O H
2. Write the IUPAC name of the major product that would be obtained from the dehydration of 3,5-dimethylcyclohexanol. What is the type mechanism of the reaction (E1, E2, SN1, SN2)? Draw the detailed mechanism of the reaction. (2.5 pts) 3. In Experiment 8, You synthesized n-butyl bromide using sodium bromide, sulfuric acid and butyl alcohol. (2.5 pts) a. Write the detailed mechanism of this reaction indicating what type of mechanism is this reaction. b. What will happen to the rate of the reaction if NaCl was used instead of NaBr? c. What will be the mechanism of the reaction if t-butyl alcohol is used with NaBr in presence of sulfuric acid? Draw detailed mechanism.
10. Draw the structural formula for the product in each of the following addition reactions for an alkene: (12 a) CH3-CH2-C=CH-CH3 + H,O CH3-CH₂ b) c) CH3 CH3-CH-C=CH-CH3 + H₂ CH3 + H₂ Pt H Ni K
CH₂OH (profic 4. True or False: Methanol reacts with HBr to form bromomethane and water via an SN1 mechanism. (3 pts) SN2
2. Draw a line structure to represent the most stable alkene formed by acid-catalyzed dehydration of 1-methylcyclohexanol. (4 pts)
(10, 6) Draw structural formulas for all of the enol forms of the carbonyl compounds below. You do not have to consider stereochemistry. Consider stereoisomeric enols as a single enol form. In the case of dicarbonyl compounds, do not include stuctures in which both carbonyl groups are present as enols.
6. (3 points) Give IUPAC names for the following compounds: CH3 с с

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man Campus Depa (a) Draw the three products (constitutional isomers) obtained when 2-methyl-3-hexene reacts with water and a trace of H2SO4. Hint: one product forms as the result of a 1,2-hydride shift. (1.5 pts) This is the acid-catalyzed alkene hydration reaction.