Draw the structure of the following three isomeric amides with chemical formula C-H₁1 NO. Amide #1: (Z)-N-methyl-3-pentenamide Amide #2: N-methylcyclobutanecarboxamide Amide #3: N,3-dimethyl-3-butenamide Consider E/Z stereochemistry of alkenes. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. + ▾ All ChemDoodleⓇ Y [F <

Draw the structure of the following three isomeric amides with chemical formula C-H₁1 NO. Amide #1: (Z)-N-methyl-3-pentenamide Amide #2: N-methylcyclobutanecarboxamide Amide #3: N,3-dimethyl-3-butenamide Consider E/Z stereochemistry of alkenes. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. + ▾ All ChemDoodleⓇ Y [F <

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...

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4. Here’s a figure-it-out mechanism, resulting in the formation of p-aminophenol from an aromatic hydroxylamine. Would you expect either ortho- or meta-aminophenol to form in competition? Why or why not? H H;0* H -N НО H2O ОН H 5. (a) The triaryl hydroxylamine hydrolyzes in acid to form two products: one compound containing two aromatic rings and one with a single aromatic ring. First, draw the two products and the mechanism of their formation in acidic water (this is another "figure it out" mechanism). Ph H;O* Ph—С—N H,0 Ph ОН (b) Suppose one of the aryl rings had a t-donating group (-OCH3) and the other had a n- withdrawing group (-NO2), both in the para position. Where would the substituents end up in the products (draw them)? Why? Do you suspect this reaction is under kinetic control or thermodynamic control, or both/either?
Which amine below is least basic? O4-Nitroaniline O Triethylamine O Pyridine O Aniline
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Hh.91.
Give the organic product: (amine) II Select one: B. III OD IV N-H + NH, Br N-H HBC IV W ? N-Br
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Draw the structure of the following three isomeric esters with chemical formula C-H1,0,. Ester #1: (E)-ethyl 2-pentenoate Ester #2: ethyl 3-methyl-3-butenoate Ester #3: (Z)-methyl 3-hexenoate • Consider E/Z stereochemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. opy aste ChemDoodle Previous Next Email Instructor Save and Exit
Draw the possible stereoisomers of 2-methylocta-4,6-dien-1-amine. Note that E-, Z- isomers of each stereoisomer are also possible and would not be accounted for by the formula above; draw any E- or Z- isomers.
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In an attempt to synthesize compound C through a two-step process, a chemist discovered after completing the first step that they had inadvertently produced two distinct compounds, A and B. Upon examining the infrared spectroscopy (IR) results, it was observed that both A and B exhibited peaks indicative of a ketone and an ester group. Please provide the molecular structures of A and B. OEt NaOEt ΕΙΟ A B In a chemical experiment, they noticed that both components, A and B, from a combined sample turned into a new compound, C, during the following stage. The task is to determine what compound C looks like and explain how compound A or B changes into compound C through a reaction. Compound C should be the primary molecule containing carbon created in this process, not just a by-product. A B H3O+, H₂O, A Mechanism = с
P Q 2 3 Write the Molar Mass? (phenylpropiolic acid) (2)-cis-Camphenic acid [(±)- cis-camphenecamphoric acid)] E-2-Chloro-3-phenyl-2- propenoic acid (trans-a- chlorocinnamic acid)