Draw a complete mechanism (including resonance structures) for the monobromination of toluene using Br_2 and FeBr_s....
1) Draw the mechanism for the radical reaction below, including potential resonance structures that explain the product distribution. Draw ALL potential products. Assume only one chlorine is attached to each product. CI 5) Draw both potential products for the reaction below. Indicate the orientation of the groups within the products in the final compounds. 6) Draw the major product for the reaction below. In 10 words or less, explain your answer. OH Excess Br-Br HO
Draw the major product and write the complete mechanism for the following reaction. Show resonance structures that lead to the formation of the major product.
5. (15 pt) a. Complete the following reaction. b. Draw a complete mechanism (include resonance structures). c. Explain the directing effect in this case using resonance structures OCH3 H3PO4 OCH3
#1. Using curved arrows to symbolize electrons, write a complete reaction mechanism for the bromination of acetanilide to create the product. Include the resonance structures for any charged, delocalized intermediates that are involved. #2. Why does performing the experiment at 0 degrees Celsius help you identify some of the relative rates of reactivity? #3. Explain why a methyl group is a mildly activating group while a methoxy group is strong activating. #4. Explain why-- NH2 act as an activator and--...
consider the resonance structures of acetanilide and methylbenzoate provided above... Several resonance structures of acetanilide are shown below: gh Resonance structures involving the amide group Resonance structures involving the aromatic n-electrons QY Resonance structures involving the aromatic T-electrons The actual electron distribution in the acetanilide molecule can be estimated considering all these resonance forms, as shown below using partial negative charges. Therefore, the nitrogen atom at the amide substituent is classified as an ortho-para-directing group. Resonance structures of methyl-benzoate and...
Draw the Lewis structure (including resonance structures) for methyl azide (CH3N3). For each resonance structure, assign formal charges to all atoms that have formal charge.
Draw a complete halohydrin reaction mechanism of cyclohexene with Br_2/H_2 O. If a stereocenter is created in the product, label that stereocenter R or S
Complete the step-by-step mechanism, including all resonance structures, for the following reaction. Show proper arrows and lone pairs for full credit. NaOH H20 НО
5. Toluene undergoes nitration at the Ortho position to produce a nonaromatic, resonance-stabilized, carbocation intermediate, which loses a proton to form a neutral substituted product. Complete the reaction mechanism below showing movement of electrons and all possible resonance structures for the carbocation intermediate. (4 points) 5. Toluene undergoes nitration at the Ortho position to produce a nonaromatic, resonance- stabilized, carbocation intermediate, which loses a proton to form a neutral substituted product. Complete the reaction mechanism below showing movement of electrons...
VI. Mechanism. (14) 1. Draw a stepwise electron pushing mechanism to predict the products in the following reduction. Make sure to show the correct locations of any deuterium (D) labels (4) 1. LA EXCESS) Co che le 2 0,09 2. Draw a complete stepwise electron pushing mechanism for the acylation of toluene below. Make sure to clearly indicate the role of the catalyst and how it is regenerated. Also clearly indicate why the methyl substituent directs the cyl group to...