2. Complete the mechanism of this Friedel-Crafts reaction below with the correct arrow pushing and missing...
1. Complete the mechanism of this Friedel-Crafts reaction below with the correct arrow pushing and missing intermediate. box 1 box 2 box 3 [pt] [1,2R] box 5 box 4 [DE] H
produce the mechanism for the friedel-crafts acylation reaction. please box the answers for these three questions. AICI3 AICI: AICI: 2 ?
Draw the product and mechanism of the following Friedel-Crafts reaction. 4. Draw the product for the following reaction. Hint: Draw the mechanism for the electrophile formation first. AICI: Followed by workup
8. Complete the following reaction by arrow pushing mechanism and identify the sequence of arrow pushing patterns. (6 pts) OH + H CI: :0- + C: I C + H2O
a) complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the Draw the structure of the organic product formed in the reaction. Draw lone pairs. conversion to the product. CH3CH2OH -CI...
5. Show a complete arrow-pushing mechanism for the following reaction. (Triethylamine is a base. It may be helpful to label carbon atoms.) (3) H3Q Et3N, heat 0 Me Me 6. Show a complete arrow-pushing mechanism for the following reaction. (4)
Arrow Pushing Mechanism Help Mechanisms & Development Provide the complete arrow-pushing mechanism for the following reaction. HT, H2O НО ОН
4. Provide an arrow pushing mechanism for the reaction below to indicate the formation of the given producto HO .. -Q. + NEN + Ci
Predict the products and provide the complete arrow-pushing mechanism for the reaction below. NaOEt EtOH
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :Ci: CH3CH2OH -Cl b) Select the option that describes the mechanism of the reaction above. O E1 O E2