5. For the following molecule: a) perform a thorough retrosynthetic analysis, including Evans-Lapworth charge affinity analysis,...
Propose a synthesis using the target molecule with
retrosynthetic analysis.
Provide complete reagents for each step of your proposed
synthesis.
from Target molecule
from Target molecule
וווו והו vide a retrosynthetic analysis to show how you would synthesize the following molecule. As starting erials you may use any alcohols of 5 carbons or less. You may use any necessary solvents and inorganic eagents. There is no need to show reaction mechanisms, just reactants, conditions and products (10 points). HyC
Retrosynthetic Analysis 12. Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. NO MECHANISMS! [8 points] NH ONH2 Make starting with
6. (12 pts) For each the molecules below, provide a retrosynthetic analysis and then give a step-by- step synthetic plan. All the carbon atoms in the final products must come from molecules in the box at the bottom. You may use any other reagents you want to accomplish your synthesis. H3CH2CO Acceptable Carbon Sources: " i hool.com ormar BCH,NH iicuch " OCH CH3
using any reagents show retrosynthetic analysis and then show
entire synthesis in forward sense
SIcP f youl proposed syninesis. from Target molecule
SIcP f youl proposed syninesis. from Target molecule
The picture below is an example of how this assignment should be
done.
This experiment involves the synthesis of a target molecule using Grignard reagents. You must do the following: 1. Perform a retrosynthetic analysis on the target molecule. The organic starting material (what you have to work backwards toward) is provided. Draw a retrosythetic scheme; use the rightwards double arrow to show functional group transformations and disconnections. Provide synthons and synthetic equivalents for every disconnection made. 2. Propose the...
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
Please help I need any idea of what to do
CHE 282- Spring 2018-Labo: Planning Multistep Synthesis of an Organic compound. 18 points Due Week of April 23 before start of Lab 10 (Late assignments penalty- 1 point per hour) Name Partner: TA: You are Student 1 Complete and submit this worksheet Attach more sheets of paper as needed L7.Leonides L7-Leonides Problem 1: Using any technique and chemical reaction(s) covered in CHE 201-202 prepare a proposed synthetic plan to show...