3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing...
1. There are three possible resonance structures of phenoxide; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 2. There are three possible resonance structures of phenyl ethanoate, draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
2. There are three possible resonance structures of phenyl ethanoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
Draw reasonable resonance structures. Use electron pushing arrow notation to show the conversion of a resonance structure into another structure.
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all resonance structures for each possible substitution position to explain why methyl m-nitrobenzoate was the favored isomer.
2. Draw electron-dot formulas for all the contributors to the resonance hybrid structures of the carbonate ion, Co2 What is the charge on each atom in each contributor? Using curved arrows, show how the electron pairs move to interconvert the three structures.
For each of the following draw all possible, valid resonance structures. Show all electron movement with arrows to receive full cred CH3 CH3 CH3
whats R? Please draw resonance structures with electron-pushing arrows for the molecule below. R) La
Consider the resonance structures of acetanilide and methyl benzoate provided above. How does the -COOCH3 substituent on methyl benzoate direct? Do the partial charges shown on either acetanilide or methyl-benzoate activate or deactivate the electrophilic substitution reaction? Is there a correlation between directing and activating groups? Explain. I Resonance structures of methyl-benzoate and the resulting partial charges are shown below. How does the benzoate group direct? 0: -1 =O :00 00 OA Several resonance structures of acetanilide are shown below:...
Three resonance structures of the following structure are possible. One resonance form is given below. Draw the remaining resonance structures, in any order, including nonbonding electrons. Omit curved arrows.
use curve arrows to indicate election motion and draw resulting resonance structures. rank the resonance structures with respect to their relative contribution to the resonance hybrid. briefly explain your choice. (12 points) Use curved arrows to indicate the electron mation and draw the resultant resonance struct ing from the structure in each case. Remember-It's a good idea to visualize the locations of the H at t aren't shown in the skeletal structures, in order to avoid drawing structures that exceed...