1) Draw another more 3-resonance forms of the following: show the movement of the arrows, and...
1) Show how you might synthesize m-bromobenzoic acid, using benzene and any suitable catalyst as your starting materials. 2) Show how you might synthesize 2-methylhexane, using acetylene and any suitable alkyl halides as your starting materials.
2. Draw all remaining resonance forms of the molecules below. Include the arrows showing electron movement between structures (6) (a) 3 additional forms (b) 5 additional forms
please help !! 3. Draw resonance forms of the following. Use arrows to show the flow of electrons. Indicate the major and minor contributor. Review E1
Draw two resonance structures for the following molecule, using arrows to show the movement of electrons.
2. Draw all the resonance forms for the following compounds. Use curvy arrows to show the flow of electrons. (8 pts)
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
can someone help me pinpoint where i went wrong? a. Draw 2 additional resonance structures using arrows to show the movement of electrons. Include any formal charges. (Hint: involve the indicated atoms when possible to help with part c) CH +2 Weevil Pheromone Based on your resonance forms above: b. What is the hybridization of the indicated Oxygen (O)? _SO sp +1 3 What must be the true hybridization of the indicated Carbon (C)? S0 C. What is its molecular...
Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. Draw the mechanism for the following transformation. Include all relevant resonance structures. Show the movement of electrons with arrows. (14 points) Pro excess HBr Br
3. For a) [CH3CH2C(-O)CH2l b) [CH3NHCHCHCH21 1) Draw their possible resonance forms as the Line-Angular structure. 2) Predict the product of the acid-base reaction between more stable resonance forms. Use the curved arrow to show the movement of electrons 3) Predict the product of the acid-base reaction between less stable resonance forms. 4) After comparing the reaction mechanisms and its products of 2) and 3). describe your opinion on the difference of stability of product. 3. For a) [CH3CH2C(-O)CH2l b)...
For each of the following draw all possible, valid resonance structures. Show all electron movement with arrows to receive full cred CH3 CH3 CH3