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- Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. N. H. 1. H3O*, heat 2. Neutralizing work-up Type here to searchWhat reagents would you use to convert methyl propanoate to the following compounds? a. isopropyl propanoate b. sodium propanoate c. N-ethylpropanamide d. propanoic acidDraw the major product of this reaction. Ignore inorganic byproducts and the amine side product. 1. NaOH, heat 2. Neutralizing work-up Select to Draw
- Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. 1. NaOH, heat N 1 2. Neutralizing work- upInstructions: Give an acceptable name for eachester. A. CH, CH2)CO,CH, B. COCHỊCH, C. CH₂CH₂CH₂CH₂COOCH₂CH₂CH₂ Instructions: Give the structure corresponding to each name. a. propyl propanoate b. butyl acetate c. ethyl hexanoate d. methyl benzoate Instructions: Give an acceptable name for each amide A. CH₂CH₂CH₂CH₂ NH₂ Instructions: Draw the structure of each amide. A. N,N-dimethylacetamide← Problem 43 of 46 Submit Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. 'N' 1. NaOH, heat 2. Neutralizing work-up Select to Draw
- d. Provide an arrow-pushing mechanism for the reaction. OH 1. NaOH 2. CH3CH₂ so acetaminophen phenacetinBy means of a suitable reaction, show how each of the compounds can be prepared from propionic acid. More than one step may be required. a. methyl propylamine (CH3NHCH2CH2CH3)b. propionyl chloridec. ethyl propionated. propionic anhydridee. N-methyl propionamide20:32 hydroxide 2. Using curved arrows, show the deprotonation mechanism of phenol with (OH). Also, provide the structure of the product of this deprotonation. Start answering this question by drawing the structure of phenol. Then hydroxide ion. Find your most reactive electrons and draw the curved arrow that shows where they would go to deprotonate phenol. Then "make a bond break a bond" write they question 3. Provide valid resonance structures for the product of the previous arrow(s) charge moving onto the ortho- and para positions. Use curved to show how the charge resonates to the next structure in your scheme. all the proper notations for depicting resonance. that show the in the structures Be sure to use Send a chat C
- Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. 1. NaOH, heat H 2. Neutralizing work-up Drawing Problem 6 Atoms, Bonds and Rings Draw or tap a newWhich of the following product(s) would not be a side product if aniline is brominated without the protection of its amino group? A 3-bromoaniline D. 3,5-dibromoaniline B. 24,6-tribromoaniline O A and D O C. 2.4-dibromoaniline O Band CFor the structure shown at the right, what type of compound is it? A. an ylide B. a nitrile C. a cyanohydrin D. an imine E. None of the selections are correct