2. Draw electron-dot formulas for all the contributors to the resonance hybrid structures of the carbonate...
14. Give the electron dot structure of the carbonate ion, CO;?, showing all possible resonance structures.
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
For each of the following anions, draw all possible resonance contributors. Show the conversion between resonance contributors by including curved arrow formalism. 1. O2N Based on the resonance structures you drew in question 1, which compound (A or B) would you expect to be the more stable anion? Briefly explain your choice. 2. Looking at the compound you chose in part 2, which of its resonance contributors is the major contributor? Briefly explain. 3.
1. Add curved arrows to both structures to show the delocalization of electron pairs needed to form the other resonance contributor. 2a.) Draw the predominant resonance contributor for the following compound; include lone pairs of electrons, formal charges, and hydrogen atoms. b) Add curved arrows to both structures to show the delocalization of electron pairs.
Part B The main resonance contributors of nitrobenzene are shown below. Use curved arrows to show how each contributor can be converted into the next. More than one arrow can be used per structure. You will need a total of four curved electron arrows to answer this question. H + N Edit the reaction by drawing all the required electron flow arrows. Electron flow arrows should start on an atom or a bond and should end on an atom, bond,...
3. Draw the important resonance contributors for each structure below (Hint - only 3-4 required for each). Include resonance arrows as necessary, and use the curved arrows to show electron movement. Also be sure to show all relevant lone pairs and formal charges. :0: H3CNCH CH3
Draw the resonance contributors that correspond to the curved, two-electron movement arrows in the resonance expressions below. Then identify the type of resonance motion in each structure below.
1. Identify all the functional groups in the following drug molecule. I Ĥ H 2. Draw all resonance structures for the following molecule and show electron movement using arrows. Pick the structure which is a major contributor to the resonance hybrid. 3. Draw curved arrows in the following reaction to show formation of product. ::
(a) Draw two resonance structures of the cation shown, shifting only one clectron pair in each step. Be sure to include the formal charge on structures B and C. Only move one double bond. Each resonance structure should contain only one charge -a positive charge. (b) Use curved-arrow notation on the given structure A to show its conversion to structure B, and then on structure B to show its conversion to structure C. 1. Draw curved arrows to show conversion of resonance...
Draw five resonance structures for this radical anion. Please show the motion of electron pairs and bonds using curved arrows. O Θ