1. Suppose you were doing two related SNAr syntheses in lab. Draw the product of mono-substitution with the aryl amine shown.NH,+(A)EtOН, 10 mLNET3, 1 molar equivalentpermmoleO,N'NO,F.FNH2(B)ELOH, 5 mL per mmoleNET3, 1 molar equivalent`NO,Two products possible -- draw either oneand assume it's the ONLY productReaction (A):MW, g/molВР, "СDensity, g/mL Amount, molesAmount, g or mLsolidXXX1.00 g`NO2NH2O,N93.131841.02mL10 mL perELOH46.07780.789mLmmoleNET3101.19890.726mLReaction (B):MW, g/molВР, "СDensity, g/mL | Amount, molesAmount, g or mLsolidXXX1.00 g`NO2NH,219.02SolidXXX5 mL perELOH46.07780.789mLmmoleNET3101.19890.726mL(b) Suppose that after recrystallization, you magically got 0.500 g of product from each reaction.What is your % yield in each case?

The answer is in the next step.

1. Suppose you were doing two related SNAR syntheses in lab. Draw the product of mono- substitution with the aryl amine showl. NH2 (A) ELOH, 10 mL per mmole NET,, 1 molar equivalent O,N `NO2 NH, (В) ELOH, 5 mL per mmole NET,, 1 molar equivalent `NO, Two products possible -- draw either one and assume it's the ONLY product Reaction (A): MW, g/mol ВР, °С Density, g/mL Amount, moles Amount, g or mL solid XXX 1.00 g ON NO, NH, 93.13 184 1.02 mL 10 mL per ELOH 46.07 78 0.789 mL mmole NET3 101.19 89 0.726 mL Reaction (B): MW, g/mol BP, °C Density, g/mL | Amount, moles Amount, g or mL solid XXX 1.00 g `NO, NH, 219.02 Solid XXX g 5 mL per ELOH 46.07 78 0.789 mL mmole NET3 101.19 89 0.726 mL (b) Suppose that after recrystallization, you magically got 0.500 g of product from each reaction. What is vour % vield in each case?

1. Suppose you were doing two related SNAR syntheses in lab. Draw the product of mono- substitution with the aryl amine showl. NH2 (A) ELOH, 10 mL per mmole NET,, 1 molar equivalent O,N `NO2 NH, (В) ELOH, 5 mL per mmole NET,, 1 molar equivalent `NO, Two products possible -- draw either one and assume it's the ONLY product Reaction (A): MW, g/mol ВР, °С Density, g/mL Amount, moles Amount, g or mL solid XXX 1.00 g ON NO, NH, 93.13 184 1.02 mL 10 mL per ELOH 46.07 78 0.789 mL mmole NET3 101.19 89 0.726 mL Reaction (B): MW, g/mol BP, °C Density, g/mL | Amount, moles Amount, g or mL solid XXX 1.00 g `NO, NH, 219.02 Solid XXX g 5 mL per ELOH 46.07 78 0.789 mL mmole NET3 101.19 89 0.726 mL (b) Suppose that after recrystallization, you magically got 0.500 g of product from each reaction. What is vour % vield in each case?

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

pls, need assistance. take a look. would these be accurate for the reaction in the picture/directions
Please answer a and b in detail. Thank you
5.) curved arrows to demonstrate the flow of electrons pairs in each potential reaction. b.) Indicate if the reaction lie to the right or the left (circle the correct arrow direction). c.) Calculate an approximate Keq for each reaction. d.) Writ the pka values under each acid, so we can evaluate your progress better and award partial credit. d.) Finally, label th acid (A), base (B), conjugate acid (CA) and base (CB) correctly based on the direction you decided. For each reaction, perform the following tasks: a.) Complete the following reactions using the appropriat Keg %3D Direction: OH LiO он Keq %3D Direction: CH3LI HOT Но Keg = Direction: O:
K Draw the initial organic product of the Bronsted acid- base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. H3O+ Drawing Question 5 Atoms,
4) Clearly identify (circle) the most acid proton on each molecule below. OH a. b. 5) The proton transfer reaction between enolate and which of the following acids (a-e) would favor the formation of the products over the reactants? Circle the letter(s) associated with your answer(s), if any. 人。 C. d. e. OH [acid] NH3 OH NH₂ HO OH 3
Step 4b: Add curved arrows to show ethoxide deprotonating the most acidic proton. Select Draw Rings More Erase / | c H0 H H :0 : H H H H
what did i do wrong here. , it seems to be marking it wrong but i thought it needed to be protonated
Just Q2
Please answer fast i give you like.
help???
Please help me this question. Thank you
3. Answer the following questions, supporting your answers with diagrams or structures. [Hint: for each acid, draw the conjugate base] a) Which proton is the more acidic proton in the following diketone? Which is more acidic? Why? b) Which of the following substituted acids is more acidic? Why? OH CI OH