49. What major organic product would you expect to obtain when acetic anhydride reacts with CH3CH₂CH₂OH? A. CH3COOH + CH3CH₂OH B. CH3CH₂COOH + CH3CH2OH C. CH3COOCH₂CH₂CH3 + CH3COOH D. CH3COOCH₂CH₂CH3 + CH3CH₂OH 50.Arrange the following esters in INCREASING relative rates of alkaline hydrolysis I. O₂N-C6H4-COOCH3 COOCH3 A. I

49. What major organic product would you expect to obtain when acetic anhydride reacts with CH3CH₂CH₂OH? A. CH3COOH + CH3CH₂OH B. CH3CH₂COOH + CH3CH2OH C. CH3COOCH₂CH₂CH3 + CH3COOH D. CH3COOCH₂CH₂CH3 + CH3CH₂OH 50.Arrange the following esters in INCREASING relative rates of alkaline hydrolysis I. O₂N-C6H4-COOCH3 COOCH3 A. I

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Calculate the parts per million of a solution made with 0.057g Pb(NO3)2 in 6552g of water.
64. What reagent(s) will accomplish this conversion? a. EtMgBr followed by an acid wash b. EtLi followed by an acid wash Et2 CuLi followed by an acid wash с. d. Et3SiCl followed by an acid wash
Draw the organic product(s) of reaction of the alkyne above with H3O+ in the presence of HgSO4.
2. Fill in the missing reagents for the following transformations. он Br MgBr а. Но b. Br
Which approach is SAFEST for the synthesis of the following ester: ། ཚི a. ii C. + CH₂OH b. H₁₂O+ OH + CH₂OH A CI + CH₂OH d. OA OB OD + CH3CH2CH2OH
The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted amide. This reaction, known as the Ritter reaction, doesnot work with primary alcohols. a. Why does the Ritter reaction not work with primary alcohols? b. Provide an explanation for why an amide is less susceptible to nucleophilic attack than its corresponding ester.
Identify the correct reagents and conditions to perform this chemoselective reaction: H ရှုံး H Select one: Me e. Reagent(s) and conditions? a. NaBH4 b. BH3 THF Pd/BaSO4, H₂ (1 atm.), quinoline, Pb(OAC)2, MeOH d. Pd/C, H2 (1 atm.), MeOH DIBAL Me H H OH
2) The product of the reaction shown is which of the following? a. A beta-diketone b. A beta-keto ester c. A beta-aldehyde ester d. A beta-diester e. The reaction fails 1) NaOH 2) H3O+
The enolate derived from diethyl malonate reacts with a variety of electrophiles (not just alkyl halides) to form new carbon–carbon bonds. With this in mind, draw the products formed when Na+ −CH(CO2Et)2 reacts with each electrophile, followed by treatment with H2O.
Enols are quite reactive toward electrophiles than alkenes because: а. The OH group has a powerful electron-donating O resonance effect b. A resonance structure can be drawn that places a negative charge on one of the carbon atoms, making this carbon electrophilic С. The enol can react with nucleophilic carbon to form a new bond to carbon d. None of the options are correct
Acetals are often prepared during the synthetic sequence to protect the carbonyl group of an aldehyde or ketone. Such an acetal is not reactive to each of the following reagents except: a.) LiAlH4 b.) PCC(Collins) c.) H3O+ d.) RMgBr e.) NaOH
Which compound will react most rapidly with acetaldehyde? A.propylmagnesium chloride B.cyclopropyl magnesium iodide C.propenylmagnesium bromide D.propynylmagnesium bromide