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what are all the by products of this reaction
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- 2. Show the curly arrow reaction mechanism for the following process including structures of the intermediates: by-products LIAIH4 (2 equivalents) HO H-AlH then work-up HCl(aq) но. H H Tetrahedral intermediate 1 Tetrahedral intermediate 26). What is the major product of the following reactions? (A) -? coon 1). NaOH in ErOH, then H,O+ 2). 1 eqiv. NaOEt 3). 1 equiv. CH3Br 4). H₂O*, Heat COOB (Intramolecular Claison) COOE (B) CH₂ COOH (D) CH₂ (E) CH3 CH₂5- 4- 1. CH3CH₂MgBr Br 2. H₂O Mg/ether 1. iH 2. H₂O
- Provide the mechanism and product(s) of the following reactions: O₂N. CI NaOH da /NH 1. KNH₂ 2. H₂O Br2, FeBr3 NaOMe3. 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 KOHClassify each of the following organic reactions. reaction Hör H₂O 1) Hg(OAc)₂, H₂O aveau Br OH OH type of reaction (check all that apply) Odihydroxylation addition hydrogenation Dhalogenation halohydrin formation. subtraction halogenation hydrogenation addition halohydrin formation inhalation Odihydroxylation addition hydrogenation oxyhydration halogenation
- 4. Provide the mechanism for this reaction: H3C O cat H* (CH,CH,)NH -Z N CH31. Write the correck IUPAC nemes Far the Foilawing organic comPounds: Br CH3 H3C 8. Assign E an or Z configuration bi CI 2. CidssiFy the Following reagents cs either nucleaphiles or e lectraph:les: Zn, CH3NH2, HS, OHa, CH3COOH, HoSO 3. Whet are the products obtained From the addition of HBr to each of the falbuing compounds? CH3 a) + HBr > CHo +HBr- 2.9) What is the major organic product of the following reaction? COOH 2 I. II. HOOC HOOC III. IV. A) I V. +HOCH₂CH₂OH B) II CH₂CH₂ CH₂CH₂0- CCH₂CH₂C COCH₂CH₂OC O=O R=0 C) III H ? COOH -COOH -OCH₂CH₂OH D) IV
- 3. Provide mechanisms for the following reactions. OH a. 18OH b. C. HO H₂180 cat. H H₂O -C=N: cat. H* 180 →EtOH + CH3CH₂CH₂CO₂H cat. CH3SO3H NH1. 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 -OHconc. HBr HO. Br 2. (Ph)3C-OH HCI (Ph);C-CI H20 d = E1 Elimination e = E2 Elimination a = Proton transfer f = Sy1 Nucleophilic substitution b = Lewis acid/base c = Electrophilic addition g = SN2 Nucleophilic substitution The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 2.