5. Determine the products for each of the following reactions. Label each carbonyl group as either a ketone oraldehyde. (Note: DMS stands for dimethyl sulfide - CH SCH3)a.1) O3, -78°C2) DMSb.1) O3, -78°C2) DMSK

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Answered: 5. Determine the products for each of…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.28P

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complete the reaction 68
1. Draw the product formed when the following ketone reduces with NaBH4 in CH3OH. DIBAL-H (H3C)3C- (H3C)3C- A. I OH охон B. II OCH 3 C. II and III CH3OH (H3C)3C D. IV || -COOH E III -OH IV -OH
please help me with all parts of this question, it is a single question with multiple subparts
In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg« 1) because bromide is a better leaving group than acetate.
027 In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg 1) because bromide is a better leaving group than acetate. +
What is the product of the following reaction sequence? 1) NaOEt (excess) H,0, H* 1) SOCI, EtO 2) 2 CH,CH,Br heat 2) NH, OEt `NH2 `NH2 `NH2 NH2 В. C. D. A. O A O'B O D MacBook Pro G Search or type URL #3 & * $ E T Y D F G H K * CO
What is the product of a Grignard reaction? O A 2° or 3° amine with the nitrogen bound to the R group from the Grignard reagent. O A six-membered ring. O An ester that incorporates the R group from the Grignard reagent. O A 2° or 3° alcohol with the a carbon bound to the R group from the Grignard reagent. Question 5 How do you prepare a Grignard reagent? O React an organohalide with magnesium metal. O React a carbonyl-containing compound with an organohalide. O Mix an organohalide with mollen magneshum. O React a carbonyl containing compound with magnesiummetal.
3. Complete the following reaction scheme: NaBH4 H* ETOH A E 1) CH;Mgl 2) H30* 1) 2) H30* он H но OH OH PCC (1 equivalente) HO. (ехceso) H* A K 1) LDA 2) CH2L PHNHNH2 H* N H2N-NH2 KOH
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find products

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5. Determine the products for each of the following reactions. Label each carbonyl group as either a ketone or aldehyde. (Note: DMS stands for dimethyl sulfide - CH SCH3) a. 1) O3, -78°C 2) DMS b. 1) O3, -78°C 2) DMS K