An equimolar amount of the three compounds below are mixed and treated with base followedby an acidic workup.1. 1 eq. (BUOKof+NC.H.OMe2. acidic workupWhich molecule acts as the nucleophile?Enter your answer hereProvide a valid explanation... Why did you choose what you chose and not something else?Enter your answer hereWhich molecule acts as the electrophile?Enter your answer hereProvide a valid explanation... Why did you choose what you chose and not something else?Enter your answer here

step 1 3-oxobutanenitrile - act as the nucleophile.

Answered: An equimolar amount of 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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Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. Н. Problem 2 of 11 :O: NaOH Submit (
The triphenylmethyl radical is an unusual persistent radical present in solution in equilibrium with its dimer. For 70 years the dimer was thought to be hexaphenylethane, but in 1970, NMR data showed it to be A. a.Why is the triphenylmethyl radical more stable than most other radicals? b.Use curved arrow notation to show how two triphenylmethyl radicals dimerize to form A. c.Propose a reason for the formation of A rather than hexaphenylethane. d.How could 1H and 13C NMR spectroscopy be used to distinguish between hexaphenylethane and A?
(That "the" should be an "a")
C341 Chapters (Acid-base chemistry) 9.) Acid-base equilibrium. For each reaction, perform the following tasks: a.) Complete the following reactions using the appropriate curved arrows to demonstrate the flow of electrons pairs in each potential reaction. b.) Indicate if the reaction lies to the right or the left (circle the correct arrow direction). c.) Calculate an approximate Ken for each reaction. d.) Write the pKa values under each acid, so we can evaluate your progress better and award partial credit. d.) Finally, label the acid (A), base (B), conjugate acid (CA) and base (CB) correctly based on the direction you decided. Keq = Direction: OH eg HO Keq = Direction: Keq = Direction: LOH OH ONa لها LIⒸ CHgLi Page 5 of 7
1. For each of the following reactions, draw in the curved arrow(s) required for the transformation and circle the type of chemical process at play. : NH2 O.. : NH2 a. i. Circle one: proton transfer nucleophilic substitution nucleophilic attack loss of a leaving group ..O ..O OCH3 OCH3 :15: b. i. Circle one: proton transfer nucleophilic substitution nucleophilic attack loss of a leaving group 11 :i: С. i. Circle one: proton transfer nucleophilic substitution nucleophilic attack loss of a leaving group
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14. a. Label the reactive features, highlight the most reactive one, then highlight what it needs. Also, state if the reaction will start to create a carbocation, carbon radical, or carbanion, or will cause loss of aromatic character. If a carbocation, carbon radical, or carbanion starts to develop, label where that will occur. butanone + CH.MgBr followed by acid b. Use mechanism arrows to illustrate the reaction that occurs. c. If applicable, use stabilization resources to deal with the carbocation, carbon radical, or carbanion that starts to develop during the reaction, and draw the structure of any resonance-stabilized intermediate. d. Continue labeling and diagramming the reaction until you find the major stable product(s). e. Finally, state the stereochemistry of the major product(s) and use either Fisher projection or perspective formula representations to illustrate that stereochemistry.
Choose the reagents that can be used to perform the following transformation: Select one: a. "OH, H₂O ...OH e. OH b. H3O+ X c. Na₂Cr₂O7, H₂SO4 d. KMnO4, OH Both -OH, H₂O and H3O+ (separately) will work.
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Hw.11.
Which if the following species is/ are susceptible to nucleophilic and electrophilic attack?
give transformation

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