3. Explain what the evidence tells you about the type of mechanism either Snl or Sn2A. The rate doubles with 2x the nucleophileB. A tertiary alkyl halide reacts faster than a secondary alkyl halideC. The rate increases with an increase in the concentration of the electrophile

Answered: Image /qna-images/answer/91f35bda-3aea-45b7-9589-c71e67200976.jpg

Answered: 3. Explain what the evidence tells you…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.SE: Something Extra

Problem 18MP: Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions...

See similar textbooks

Similar questions

For the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Hmm.. CEN + CI Organic product Inorganic product
For the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. HI.... + CI Draw the organic product. :C=N to H Organic product + Inorganic product Draw the inorganic product. ū
In an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.
2. Draw the structures and explain why CH3CH₂O and CH3CO₂ are good nucleophiles but CH3SO3, water, and alcohols (R-OH) are poor nucleophiles. Propose a 'cutoff' for the amount of negative charge needed to be a good nucleophile. CH3CH₂O CH3CO₂ CH3SO3 H₂O CH₂OH
5. Classify the following reagents as either nucleophiles or electrophiles: Zn2* , CH3NH2 , HS , OH2 , CH3COOH, H2SO4
For the given Sy2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. :CEN Organic product Inorganic product + Draw the organic product. Draw the inorganic product. Incorrect
please do the mechanism. Identify which one is the nucleophile/electrophile. Name the reaction as well. Discuss the stereochemistry so why the dash bond go to wedged- due to inversion? Why is PPh3 used for selectivity ? Please answer all of my questions.
In halogenation reactions, why are halogens added on opposite sides of the compound? because the reaction proceeds via free radical and the pi cloud holding the electron are directed away from each other because of the formation of a halonium ion which sterically blocks one side of the compound thus the other side is open for attack because the halogen should occupy both sides to accommodate the pi clouds None of the above Two equivalents of HCl are added to an alkyne, where do you expect to see the Cl atom? The two Cl atoms will be distributed between the two Carbon atoms involved in the triple bond The two Cl atoms forms a bond with the less substituted carbon Both Cl atoms attach to one carbon, which is the more substituted one A mixture of products are formed
please do the a new mechanism. which one is the nucleophile/electrophile. And what is Name the reaction. PLEASE Discuss the stereochemistry so why the dash bond go to wedged- is it due to inversion? Please explain.Why is PPh3 used for selectivity ? Please answer all of my questions.
Use the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaCN Br CN CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaCN X: choose your answer... Y: choose your answer... Z: choose your answer... >
Use the dropdown menu to indicate whether the rate of the reaction shown below will increase, decrease, or remain the same when the reaction conditions are changed to X or to Y or to Z (see below). NaN3 'N3 Br CH3CN X: Change the leaving group from Br to CI Y: Increase the concentration of haloalkane Z: Increase the concentration of NaN3 X: choose your answer.. ^ Y: choose your answer... V Z: choose your answer... choose your answer... Remain the same Nex Decrease Increase
Draw the electron-pushing mechanism for the propagation steps of the allylic bromination reactions below. You may omit NBS in your mechanism, and use Br and Br2.

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Pushing Electrons

Chemistry

ISBN:

9781133951889

Author:

Weeks, Daniel P.

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Pushing Electrons

Chemistry

ISBN:

9781133951889

Author:

Weeks, Daniel P.

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

3. Explain what the evidence tells you about the type of mechanism either Snl or Sn2 A. The rate doubles with 2x the nucleophile B. A tertiary alkyl halide reacts faster than a secondary alkyl halide C. The rate increases with an increase in the concentration of the electrophile