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Reaction: bromobenzne ---->Mg product is MgBr attacthed to benze ring
If someone used “wet” benzophenone what product would expect instead?
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- ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) ButylamineArC#N D LIAIH/EtO 2) H (aq) b) 2 Benzophenone + bopropyl Alkohol 1) NaBHJEIOHI Hexanal 2) H"(aq) PhC CLi HC- CH: (be), H DCN, H Acetophenone 2) KOH (), AOne of the products produced when is treated CH;CH, CH,-Č-NHCH; with NaOH is O CH3-NH2 O CH3-CH2-CH2-NH2 CH3-NH3*CI" CH;-CH, -C-NH,
- What is the appropriate systematic name for the compound below? HO., SH ) (15,45)-4-hydroxycyclohex-2-enethiol O (35,65)-6-mercaptocyclohexen-3-ol )(1S,4S)-4-mercaptocyclohex-2-enol (3S,65)-6-hydroxycyclohexene-3-thiolShow how you would synthesize the alcohol shown, from an alkene and the reagents provided. Draw the alkene and select a reagent. ОН reagent alkene Draw the starting alkene. Select the reagent needed. Select Draw Rings More Erase C H NaOH, H,O 1. BH3; 2. H,O, NaOH 1. Hg(OAc),, H,O; 2. NaBH, Question Source: Organic Chemistry: Structure And Function 7e | Publisher: MacBook ProWe your anver on paper and submit a picture here gir emaitto me ty the end of pe time for he exam CHOH CH.OH CHOH HA Provide a step-wise mechanism for the following equation, show intermediates and arrows for exchange of electrons.
- 2) Provide the major organic product(s) for each of the following reactions. You may ignore drawing stereoisomers if formed. ( NH H2O, pH 6 2) 3) H3O* 1) NaOH, H2O H. 2) But-3-en-2-one (provide structure for product) 1) NaOEt, HOET 2) H3O* 1) NaOEt, HOEt 2) 3) H3O* 1) (CH,CH,CH,),CuLi THF, -78°C 2) CH3BrNot all aldehyde give a positve Bendicts test. Which of the follwing aldehydes do? a. d. b. e. c.O (1) H20, H*; (2) Jones reagent (1) H20, H*; (2) PCC, CH2CI2 (1) conc. H2SO4: (2) Jones reagent O (1) H20, H*; (2) Tollens reagent (1) conc. H2SO4: (2) PCC, CH2CI2 O (1) conc. H2SO4: (2) Tollens reagent
- For each IUPAC name, draw the complete structure. (a) (25,3R.4R)-2,3-diamino-4-hydroxycyclopentanone; (b) (2R.3R)-2-butyl-3-hydroxypentanedial: (c) (4S,5R)-4.5-diaminoheptane-2,3,6-trione: (d) (3E,5R,6Z)-5-hydroxy-7-methoxyocta-3,6-dien-2-oneua U LIIUUSE une correct name tor each structure shown. [ Select) H. CH3 [ Select ] a- OH O CH) HO-E-E- -CH,-CH, CH, [ Select ) V [ Select ] CH-CH,-CH2-C-o-CH, methyl butanoate methyl carboxybutane butyl methanoate CH,-CH-NH-CH, CH, methyl butyl ester H3CN-CH3 'N' [ Select ) [ Select ) H. CH3 -OH [ Select ] CI O CH, HO-C -CH,-CH, [ Select ) ČH, ( Select ) CH,-CH, -CH2-č-o-CH, CH,-CH-NH-CH, V[ Select ] CH, 1,1-dimethylbenzne dimethyl-nitro-benzene H3C CH3 N. 1,1 dimethylcyclohexane N-methyl-2-propanamine [ Sel [ Select ] CH3-CH2-CH2-c-o-CH, CH3-CH-NH-CH; ( Select ] ČH3 H3C., -CH V [ Select ] dimethyl-nitro-benzene 1,1 dimethylcyclohexane N,N - dimethylaniline 1,1-dimethylbenzne NH, [ Select) H,C. NH, [ Select ] CH3-CH2-C-NH - CH,Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. (M) CH3 M oxidation 2req SH reduction M M) • You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. (M) C. P. aste opy M) = 2req s 2req M) M) ts ChomDondlo