Please show the most acidic compound and explain all the reasons why it's more acidic ROR...
Explain why compound A is more acidic using resonance structures and question 21. WILLUDUlyalli Clemsty ENAM 20. Explain why Compound A is more acidic than Compound B. Use resonance structures to e 21. Which of the following is the least stable carbocation? Circle your response. (2) IV
7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) Acidity of one pf the it's shown 8. For the reaction show, a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures for the intermediate (4 pts) Br...
11) Which compound is most acidic ? Explain. NO2 O O -COH сон COM "OCH3 12. Predict the major product. CH3 CH3 -NH₂ 1.) CH₃ I 2.) AgzO/ H₂0² 13.) Predict the product, Show each step. 1.) Febrz/Bra 2.) H2SO4/ HNO3 7 3.) HCI / NaNO2 4.) H₂ot
Which compound is stereochemically equivalent to idose? Please explain and show all work. Select one: a. a b. b c. c d. d HO OH OH OH HO HOOH HO HO H HO HO HO HO OH; (a) HO (b) HQ c) HO (d) HO HO HO HO H idose OH H HO
please answer will rate Which is the most acidic hydrogen in the following compound? V o H HAI CN H HII IV H Hн A. III B. I C. II D.V E. IV
2.2 Nitromethane (CH3NO2, pka = 10) is more acidic than most organic acids. Explain why nitromethane is so much more acidic than ethane (pka = 60). Write the chemical equations to illustrate the acidity of the compounds. Include valid Lewis dot structures (including formal charge) and resonance structures, if relevant. (6)
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
7-9 please! 4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
17. Select the most acidic hydrogen in the compound shown below: A. HO C. H B. D. H + 0 18. Addition of methyl lithium to the enone below generates the product shown after treatment with acid and water. Select the key intermediate in the mechanism for the last step: ОMe H2O Meli H2SO4 H,to bar ne you laus to A.
Can anyone explain why it's FeCrO4 instead of Fe2(CrO4)2? please explain more details as possible, i will give upvote. Write the empirical formula for at least four ionic compounds that could be formed from the following ions: Fe2+, Fe3+, CroC,H,02 C,H02 Croz Fe3+Fe(C2H,02), Fez (C+04) Fe2+Fe(C2H,02), FeCrO 4