HO(c) (1 pt) Both of the following are hydride donors. Circle the harder nucleophileof-P-Cu-HH+H-AI-HH(d) (4 pts) The following reaction involves two steps. Draw the anionic intermediate thatforms after sodium hydride reacts and the final organic product.Hints: what type of nucleophile is NaH and where does that mean it will react? Also, thesecond step is not a proton transfer. What's the most likely reaction for that intermediateto undergo?NaHanionic intermediatefinal product

In general, a 'hard' nucleophile is one that is small, highly charged, and does not have accessible…

Answered: HO (c) (1 pt) Both of the following are…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter20: Acidity And Pka Of Phenols

Section: Chapter Questions

Problem 11E

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One of the steps in the mechanism of the above reaction as shown below. Draw the structure of all the products of this reaction. com/mm/takeAssignCourt Rotivity.do?locator assignment-take 1 pt ment Eto O Eto O 3. NaOH, H₂O, heat 4. HCI, H₂O, heat One of the steps in the mechanism of the above reaction is shown below. Draw the structure of all of the products of this reaction. O OEt O 1. Eto Na 2 Å OH You do not have to consider stereochemistry. • Draw enolate anions in their carbanion form. . You should include all products. Ôno P Ć [References) . Include counter-ions, e.g., Na, I, in your submission, but draw them in their own separate sketcher. . Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate multiple products using the + sign from the drop-down menu. ///-000- IF Previous Email Instructor
Rank the following compounds towards nucleophiles. (1-most reactive - 4- least reactive)
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6. The following reaction is an example of OH A) SN1 B) SN2 Br NaOH EtOH C) E1 D) E2 7. In the above reaction (Q6), what is the role of NaOH? A) It acts as an acid and reacts with EtOH B) It acts as nucleophile and attacks on electrophilic carbon in bromoprop C) It acts as a base and reacts with phenolic OH and forms phenolate ion D) It acts as a spectator
Which sequence of reactions will complete the transformation below? 1) BH3-THF, 2) NaOH, HOOH, 3) NaOEt 1) HBr, 2) ethanol, heat 1) BH3-THF, 2) HOOH, NaOH, 3) NaH (strong base), 4) ethyl iodide 1) HBr, ROOR, heat, 2) NaOEt OHBr, ethanol, heat LOCH₂CH3
5. Write a detailed chemical mechanism for the following reaction. [10 pts] NBS hv ? For full credit, • Explicitly label initiation, propagation, and termination steps. • Use 'curly arrows' to denote electron flow. Show all resonance forms of the reaction intermediate(s). N-Br NBS (N-bromosuccinimde) • Show reaction at any resonance forms of the reaction intermediate(s) that lead to different products. including constitutional and stereochemical isomers (if any). Show two different termination steps. Showing more steps will not earn points; wrong steps will lose points

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