IT). A. Write a chemical equation for the formation of 1,2-dimethoxy-4-nitrobenzene from the reaction of 3,4-dichloronitrobenzene...
m. A. Write a chemical equation for the formation of 1,2-dimethoxy--nitrobenzene from the reaction of 3,4-dichloronitrobenzene with two equivalents of sodium methoxide. IT. B. Draw resonance structures for the anionic intermediate that would be produced by the reaction of methoxide ion at the 3-position of 3,4-dichloronitrobenzene. II. C. Draw resonance structures for the anionie intermediate that would be produced by the reaction of methoxide ion at the position of 3,6-dichloronitrobenzene. 4
answer questions a, b and c please I). A. Write a chemical equation for the formation of 1,2-dimethoxy-+-nitrobenzene from the reaction of 3,4-dichloronitrobenzene with two equivalents of sodium methoxide. IT). B. Draw resonance structures for the anionic intermediate that would be produced by the reaction of methoxide ion at the 3-position of 3,4-dichloronitrobenzene. IT). C. Draw resonance structures for the anionic intermediate that would be produced by the reaction of methoxide ion at the 4-position of 3,4-dichloronitrobenzene. 4
I). A. Write a chemical equation for the formation of 1,2-dimethoxy-4-nitrobenzene from the reaction of 3,4-dichloronitrobenzene with two equivalents of sodium methoxide.
Draw the structure of the organic product formed from the reaction of sodium methoxide with 1-chloro-4-nitrobenzene. Be sure to show formal charges.
This is the chemical equation 4. Write the balanced chemical equation for the formation of the (S.S.S)-bis-proline phenylsuccinic acid salt and the (S,R,S)-bis-proline phenylsuccinic acid. Start with 4 y equivalents of (S)-proline and two equivalents of racemic phenylsuccinic acid. (1.0 point). 5. Write the balanced chemical equation for the formation of (S)-phenylsuccinic acid. Start with one equivalent of (5.5.S)-bis proline phenylsuccinic acid salt and two equivalents of hydrochloric acid. (1.0 point). 6. Draw the full arrow.pushing mechanisms for the equations...
4. Write the balanced chemical equation for the formation of the (5.5.5)-bis-proline phenylsuccinic acid salt and the (S,R,S)-bis-proline phenylsuccinic acid. Start with 4 equivalents of (S)-proline and two equivalents of racemic phenylsuccinic acid. (1.0 point). 5. Write the balanced chemical equation for the formation of (s)-phenylsuccinic acid. Start with one equivalent of (S.5,5)-bis proline phenylsuccinic acid salt and two equivalents of hydrochloric acid. (1.0 point). 6. Draw the full arrow-pushing mechanisms for the equations in questions 4 and 5 a....
help please! 13) Write a rational mechanism for the reaction of 3,4-Dichloronitrobenzene with Sodium Methoxide (30 points) 14) Indicate the limiting reagent and calculate the percent yield in the following reaction (30 points) NH2 NHCCH3 i + CH3C-0—CCH3 OH p-aminophenol OH acetaminophen p-aminophenol: molecular weight = 109.13 g/mol; grams utilized=0.6 acetic anhydride: molecular weight = 102.09 g/mol; density = 1.08 g/mL; mL utilized = 0.70 acetaminophen: molecular weight = 151.17 g/mol; grams obtained = 0.62 15) If lane 1 is...
Write the balanced chemical equation for the formation of magnesium oxide from magnesium and elemental oxygen. 1. Write the balanced chemical equation for the formation of magnesium nitride from magnesium and elemental nitrogen. 2. Write the balanced chemical equation for the conversion of magnesium nitride to magnesium oxide as performed in steps 7-8 in the procedure. The reaction produces magnesium oxide and ammonia (NH,). 3. If some of the product contained magnesium nitride rather than magnesium oxide, would the experimental...
Write a balanced chemical equation for the formation of a dimer via a condensation reaction from one molecule of succinic acid (HOOCCH2CH2COOH) and one molecule of ethylenediamine (H2NCH2CH2NH2)
A) write the balanced equation for the reaction of vanillin with h2o2 to give divanillin. B) The first step in the mechanism of this reaction involving vanillin is the formation of phenoxy radical by the abstraction of phenolic H atom. Draw all the neutral resonance structures of this vanillin phenoxy radical. Draw atleast 5. Which resonance structure leads to the divanillin?