Which of the following methods does not work to synthesizebenzoic acid?CrO3, H2SO4, H,OA) C,HSCH2OHMgCO2НB) C,H5BTNaCNНО, НC) C,H5B.Na,Cr,O;D) C,HSCH3H2SO4, H20A

Benzoic acid is a derivative of benzene containing -COOH functional group. It is usually prepared by…

Answered: Which of the following methods does not…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter23: Addition To A Carbonyl

Section: Chapter Questions

Problem 24E

See similar textbooks

Similar questions

Show a possible mechanism for the following reaction 1) EtMgBr (еxcess) 2) H20 Et OH Me •Me "Et w..
Which is the best reaction sequence to synthesize m-bromobenzenesulfonic acid from benzene? Br ex OH 1) CH3CI, AIC13, 2) Br2, AlBr3 1) ethene, HF, 2) Br2, FeBr3 1) Br2, FeBr3, 2) H2504 1) Br2, FeBr3, 2) CH3COCI, AICI3 1) H2SO4, heat 2) Br2, FeBr3
Draw the organic products formed in attached reactions?
H₂C H₂C لیے CH–COOH +CH,CH(CH,)NH, H₂C heat 2 Reaction D Select Draw Rings More Erase / |||||| CON H COOH +CH,CH(CH,)NH₂ CH3 Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) (CH3CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. heat G Q2Q
2) Show the product(s) & intermediates for the following reactions. a) d) H 1) MgCH 2) H2SO4 OH PCC DMP CH,α, 2 d) 1) disiamylborane 2) H₂O2, NaOH 1) LIAIH(Or-Bu)3, 2) H₂O
L 15. Draw the mechanisms for these reactions. ( O acid a. + H₂N—OH он EN OH 1 + H₂O b. base + H₂C=O A C. O TSOH + 2 CH₂OH BO 4 + H₂O - 0. 0- + H₂O " - " H
3) Complete the following: Stereochemistry and regiochemistry may be important. b) d) type type MeO Br type type type OH H Br E1 Reaction Borohydride Reduction H NaOAc DMF Асон HO PCC CH₂Cl2 H CO₂Et f) g) h) i) j) type type type type type OH OH Hydride Reduction MeHN Reductive Amination HO Br OH
As far back as the 16th century, South American Incas chewed the leaves of the coca bush, Erythroxylon coca, to combat fatigue. Chemical studies of Erythroxylon coca by Friedrich WĂ¶hler in 1862 resulted in the discovery of cocaine, C17H21NO4, as the active component. Basic hydrolysis of cocaine leads to methanol, benzoic acid, and another compound called ecgonine, C9H15NO3. Oxidation of ecgonine with CrO3 yields a keto acid that readily loses CO2 on heating, giving tropinone. (a) What is a likely structure for the keto acid? (b) What is a likely structure for ecgonine, neglecting stereochemistry? (c) What is a likely structure for cocaine, neglecting stereochemistry?
Which of the following best represents a mechanistic step in the acid-catalyzed hydrolysis of acetonitrile? А) НС —СEN: Н-ӧ: Н В) НС —СN-H Н-ӧ: н С) НС —СN: н ӧ: D) H3C-C=N: Н-ӧ: н
Will the following bases favor an E1 or E2 mechanism? H2O, CH3CO2^-, tBuO^-, CH3CH2OH, -NH2, NaH
Draw Reaction mechanism for ephedrine. Left one is the example for aspirin
complete the reaction 68

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

Which of the following methods does not work to synthesize benzoic acid? CrO3, H2SO4, H,O A) C,HSCH2OH Mg CO2 Н B) C,H5BT NaCN НО, Н C) C,H5B. Na,Cr,O; D) C,HSCH3 H2SO4, H20 A