Draw the structures of the produce(s) formed in the alkylation reactions, showing the mechanisms
In the boxes provided draw the structures of the organic products formed in the following reactions.I need to see the mechanisms for the answers.
In the boxes provided draw the structures of the organic products formed in the following reactions.I need to see the mechanisms to get the products.
In the boxes provided, draw the structures of the cyclic organic products formed in the following reactions.I need to see the mechanisms to get the answers.
S. Answer ALI. parts (a) Draw structures for compounds G-L. formed in the scheme below HBr 1 HBr, peroxides 0) 0s04 il) NalHSO, Cly, H20 (b) Write mechanisms for the reactions leading to compounds G, H and K above. Devise a reaction sequence for achieving the conversion: (12) (c) Give reagents and conditions and draw the structures of the intermediate compounds formed. Reaction mechanisms are not required
Draw the structures of the intermediate carbocations in the alkylation of naphthalene, the active ingredient of moth balls. Why does naphthalene undergo electrophilic substitution at C1 rather than C2? Draw resonance structure(s) to justify your statement.
Draw the structures of the initially formed enol tautomers in the reactions of propyne and dicyclohexylethyne with dicyclohexylborane followed by NaOH and H_2O_2.
Draw the structures of the expected organic product(s) formed in the following reactions including correct stereochemistry. If more than one product is possible draw all products and write major or minor product where necessary. Indicate what the mechanism of the reaction is. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'. DMF = dimethyl if ormamide, CH_3 CN = acetonitrile
Draw both resonance structures of the enolate formed when each of the following ketones is treated with a strong base. Show mechanisms.
16. Draw a mechanism to show how two alkylation products are formed in this reaction. a. LDA b. CHI 17. Briefly explain why reactions that use LDA as a base must be carried out in anhydrous conditions (ex. inert atmosphere).
For the Friedel-Craft alkylation reactions below, predict if and where alkylation will occur. Draw the structure of the major product for each reaction by hand or write in "no reaction". Briefly why your selection was made for each reaction. (12 pts) NO a. AICI, Br in excess AICI, O. in excess AICI Br in excess
For the Friedel-Craft alkylation reactions below, predict if and where alkylation will occur. Draw the structure of the major product for each reaction by hand...