(a)
Interpretation:
Plausible mechanism should be drawn given the major product of 2-methyl-2-hexene.
Concept Introduction:
E2 reaction is a bimolecular elimination reaction in which alkene compounds formed in a single step.
Rate of E2 reaction is depends upon the concentration of substrate and concentration of base. Because in a bimolecular reaction, there should involves two chemical entities.
Equation for the rate of E2 reaction is,
(b)
Interpretation:
The expected rate equation should be found for the given reaction.
Concept Introduction:
E2 reaction is a bimolecular elimination reaction in which alkene compounds formed in a single step. Alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide.
Rate of E2 reaction is depends upon the concentration of substrate and concentration of base. Because in a bimolecular reaction, there should involves two chemical entities.
Equation for the rate of E2 reaction is,
(c)
Interpretation:
The change in rate when concentration of base is doubled in given reaction has to be explained.
Concept Introduction:
E2 reaction is a bimolecular elimination reaction in which alkene compounds formed in a single step. Alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide.
Rate of E2 reaction is depends upon the concentration of substrate and concentration of base. Because in a bimolecular reaction, there should involves two chemical entities.
Equation for the rate of E2 reaction is,
(d)
Interpretation:
Energy level diagram should be drawn for the given reaction process.
Concept Introduction:
E2 reaction is a bimolecular elimination reaction in which alkene compounds formed in a single step. Alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide.
Energy diagram of an E2 reaction has only one hump because only one step is involved in the E2 reaction.
Transition state is a state in between the reactant and product.
In the transition state of E2 reaction: the abstraction of β-proton by the base, removal of leaving group (halo-group) and formation of double bond are taking place.
(e)
Interpretation:
The transition state should be drawn for the given transformation of reaction.
Concept Introduction:
E2 reaction is a bimolecular elimination reaction in which alkene compounds formed in a single step. Alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide.
Energy diagram of an E2 reaction has only one hump because only one step is involved in the E2 reaction.
Transition State: The state which defines the highest potential energy with respect to reaction co-ordinate between reactant and product. It is usually denoted by using the symbol ‘≠’.

Want to see the full answer?
Check out a sample textbook solution
Chapter 7 Solutions
Organic Chemistry
- curved arrows are used to illustrate the flow of electrons. using the provided starting and product structures, draw the cured electron-pushing arrows for thw following reaction or mechanistic steps. be sure to account for all bond-breaking and bond making stepsarrow_forwardUsing the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.arrow_forwardSynthesis of Dibenzalacetone [References] Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. Question 1 1 pt Question 2 1 pt Question 3 1 pt H Question 4 1 pt Question 5 1 pt Question 6 1 pt Question 7 1pt Question 8 1 pt Progress: 7/8 items Que Feb 24 at You do not have to consider stereochemistry. . Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 4arrow_forward
- Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)arrow_forwardHi I need help on the question provided in the image.arrow_forwardDraw a reasonable mechanism for the following reaction:arrow_forward
- Draw the mechanism for the following reaction: CH3 CH3 Et-OH Et Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H± EXP. L CONT. י Α [1] осн CH3 а CH3 :Ö Et H 0 N о S 0 Br Et-ÖH | P LL Farrow_forward20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?arrow_forward20.00 mL of 0.025 M HCl is titrated with 0.035 M KOH. What volume of KOH is needed?arrow_forward
- 20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?arrow_forward20.00 mL of 0.025 M HCl is titrated with 0.035 M KOH. What volume of KOH is needed?arrow_forward20.00 mL of 0.150 M HCl is titrated with 37.75 mL of NaOH. What is the molarity of the NaOH?arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





