2. Complete the following: Stereochemistry and regiochemistry may be important.typea) NaOH (aq)b) neutralize ➤OMea) LiAlH4, etherNMe2f)b) H3O+typeb)a) HSSHZnCl2, H+b) Raney Nig)type formation of thioacetal/desulfurizationHOtypeHell-Volhard-Zelinsky Reactionh)CO₂EttypeWittig ReactionHH₂NOEtOHDCC, CH2Cl2Phtypea) NaH, THFCO₂Etd)b) BnBr, THECO₂Etc) NaOH(aq); HCl(aq); heattypetypeHOtype(COCI)2, cat DMFCH2Cl2j)CItypea) NHENb) LiAlH, THEc) H3O+CO₂MeCO₂Me

References; Bodé, N. (2018). Exploring undergraduate organic chemistry students' strategies and…

Answered: 2. Complete the following:…

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

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.69P

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2) Complete the following: Stereochemistry and regiochemistry may be important. a) b) C) d) e) type type type OCH 3 type type OH CH₂OH EAS - Nitration H₂ Lindlar Catalyst KMnO4 NaOH/H₂O + OCH3 "OCH 3 Br CHO OH OH f) g) h) i) j) type type OCH3 type type type OH Bronsted-Lowry acid base chemistry CO₂Me OH K Friedel-Crafts Acylation NO₂ a) LIAIH,₁, ether b) H₂O* H₂SO4 OH OH NH₂
Complete the following: Stereochemistry, enantio-, and regioselectivity are important. CrO3, H2SO4 a) OH Bromination of an alcohol (Sn2) type EtO₂C CO₂Et b) b) d) H3CO type NH2 a) b) H3CO type a) b) OH g) type CN CI h) acetone Swern Oxidation type type CO₂H type Доно i) Me3SICI, Imidazole OSiMe3 Et3N, CH2Cl2 Br type a) Mg°, THF Br j) b); H3O+ H2SO4 (H+) MeOH OMe type type
please draw out solutions
a) b) c) d) e) 1) BH3/THF 2) H₂O2 NaOH (aq) cold Cl₂, H₂O HBr CH3CH₂OOCH₂CH3 1. Hg(OAc)2, H₂O 2. NaBH4 o 1) 03 (-78 °C) 2) (CH3)S H₂ Lindlar catalyst
Please help with part A, B, C, D
Please help with part A, B, C, D:
Please help with part J, H, I and J:
3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOH
3. Explain, giving structures of important reaction intermediates and transition states, the stereochemical outcome of each of the following reactions. a) & 1) LDA/THF/-78°C 3) acidify (cold) R major (racemic) OH Ph + minor (racemic) OH Ph
please help with part g, h, i and j:
Give the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal Br a) 2) NaCN, acetone 1) NaOC(CH3)3, heat d Br 2) BH₂ THF; 3) H,O,, NaOH(aq) b) c) d) c) 2) KOC(CH3)3, heat Copyright University of California Merced 2022 Br 1) NaOH, heat 2) MCPBA 1) KOC(CH3)3, heat 2) H3O+
5. Provide the structures as necessary to complete the following sequences of reactions. Indicate stereochemistry when needed and if more than one stereoisomer can be formed just draw one of the stereoisomers unless otherwise indicated. Only organic products need to be provided. a) (excess) 1) 03 2) H202 b) Pd/C CO,Me H2 c) 1. NaH H2 2. Pd/Baso4 quinoline Br

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