6. Plan a synthesis of each of the following targets from benzene and write the forward...
6. Plan a synthesis of each of the following targets from benne and write the forward Syntheses in each box below. To depict a synthesis in the forward direction, draw each reaction with conditions above or below an arrow, draw the structures of all isolated Synthetic intermediates not reactive intermediates and include the structure of the target at the end. Note: more than one route may be possible Homework CHEM 2313 Fall 2019
What are the following syntheses for each compound? 7. Propose a synthesis for each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. осон steps H₂C (ra (racemic) Hoc OH Hac CH3 сна N-OH steps
2. Propose a synthesis of the following molecule from benzene. Show the product of each individual step in your synthetic route. Use whatever reagents are required.
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...