Instead of propanoic acid, show using
propanol please
Homework Answers
Add Answer to:
Instead of propanoic acid, show using
propanol please
5. Synthesis: Show how the amine could be...
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine....
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited access to any inorganic reagent. and OH and
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine....
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited access to any inorganic reagent. Он and and 6. Give all possible structures of the product (C20H1203) formed by intramolecular Claisen condensation of the keto-ester shown below. 1. NaOH 2. H30 Page 3 of 4
synthesis show how the immune could be prepared from benzene propanoic acid and dimethylamine. More than...
synthesis show how the immune could be prepared from benzene
propanoic acid and dimethylamine. More than one synthetic
transformation will be necessary
give all possible structures of the product C 10 H 1203 form
by intermolecular placing condensation of the keto Ester shown
below
ps * Bookmarks Gmail YouTube Maps Ch15: Oxidation o. 5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited...
Please provide a Bayer-Villiger oxidation reaction mechanism for synthesis of propanoic acid 1,1-dimethylethyl ester from 2,2-dimethyl-pentan-3-one,...
Please provide a Bayer-Villiger oxidation reaction mechanism for synthesis of propanoic acid 1,1-dimethylethyl ester from 2,2-dimethyl-pentan-3-one, solvent:H20 and reagent m-chlorobenzoic acid.
1. Show how you could make the amine shown by Reductive Amination and by Acylation and...
1. Show how you could make the amine shown by Reductive Amination and by Acylation and then reduction. Clearly show the starting materials and reagents for each approach Q Target amine: 2. Devise a synthesis of the target amine from question one starting from Toluene (methyl benzene) and any two carbon compounds you wish. 3. Propose a synthesis of this azo dye starting from Benzene and acetic acid as your only source of carbons. Target Dye: 4. Can you rationalize...
Show, by writing a series of synthetic steps how you could prepare the following target compound...
Show, by writing a series of synthetic steps how you could prepare the following target compound for the designated two starting materials (a cyclic diene and acetylene) and any other necessary organic or inorganic reagents. You must also show all the intermediate structure(s) for your synthesis indicated by the "?" marks. More than one step will be needed. H CH,CH, CH CHH + H-C=C-H ? ?
Show how you could prepare each of the following carboxylic acids using Grignard's reagent: OH from...
Show how you could prepare each of the following carboxylic acids using Grignard's reagent: OH from benzene OH + from 1-bromo propene and acetone он from 3-bromoprop-1-ene 4-Methylbenzoic acid from benzene
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as...
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as your ONLY sources of carbon atoms. More than one step is required. You do NOT need to show the mechanism. You can use any other reagents that you desire. [6 marks]
Multistep Synthesis (9 pts) Show how to convert benzene into at least one of the molecules...
Multistep Synthesis (9 pts) Show how to convert benzene into at least one of the molecules below using any reagent. You should be able to do this in three steps but this is not a required minimum or maximum. If you are not sure of an intermediate step put down structures and as much as you know about reagents to maximize partial credit. You may attempt more than one and the best will be graded. It is ok if a...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited access to any inorganic reagent. and OH and
5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited access to any inorganic reagent. Он and and 6. Give all possible structures of the product (C20H1203) formed by intramolecular Claisen condensation of the keto-ester shown below. 1. NaOH 2. H30 Page 3 of 4
synthesis show how the immune could be prepared from benzene
propanoic acid and dimethylamine. More than one synthetic
transformation will be necessary
give all possible structures of the product C 10 H 1203 form
by intermolecular placing condensation of the keto Ester shown
below
ps * Bookmarks Gmail YouTube Maps Ch15: Oxidation o. 5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited...
1. Show how you could make the amine shown by Reductive Amination and by Acylation and then reduction. Clearly show the starting materials and reagents for each approach Q Target amine: 2. Devise a synthesis of the target amine from question one starting from Toluene (methyl benzene) and any two carbon compounds you wish. 3. Propose a synthesis of this azo dye starting from Benzene and acetic acid as your only source of carbons. Target Dye: 4. Can you rationalize...
Show, by writing a series of synthetic steps how you could prepare the following target compound for the designated two starting materials (a cyclic diene and acetylene) and any other necessary organic or inorganic reagents. You must also show all the intermediate structure(s) for your synthesis indicated by the "?" marks. More than one step will be needed. H CH,CH, CH CHH + H-C=C-H ? ?
Show how you could prepare each of the following carboxylic acids using Grignard's reagent: OH from benzene OH + from 1-bromo propene and acetone он from 3-bromoprop-1-ene 4-Methylbenzoic acid from benzene
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as your ONLY sources of carbon atoms. More than one step is required. You do NOT need to show the mechanism. You can use any other reagents that you desire. [6 marks]
Multistep Synthesis (9 pts) Show how to convert benzene into at least one of the molecules below using any reagent. You should be able to do this in three steps but this is not a required minimum or maximum. If you are not sure of an intermediate step put down structures and as much as you know about reagents to maximize partial credit. You may attempt more than one and the best will be graded. It is ok if a...
Show how you would accomplish the following synthesis, in good overall yield, using the indicated starting materials and any other necessary reagent(s) (as long as these are involved in reactions presented/reviewed in course notes/lecture videos). State clearly all required reagents and conditions (if these are important for the outcome of the reaction). There is no need to provide mechanistic details or to show retrosynthetic analysis. (Important: please, keep in mind that submission of unnecessary content that is incorrect will be...
Most questions answered within 3 hours.
-
Write a program to solve the Josephus problem, with the following
modification:
Sample Input:
./a.out n...
asked 32 minutes ago -
At the start of a CD it is spinning at a rate of 525 rpm
(revolutions...
asked 1 hour ago -
4. Without doing any calculations, predict whether the observed
∆T would increase, decrease or remain the...
asked 2 hours ago -
Based on the range, which of the following sets of scores has
the greatest variability? 3,...
asked 3 hours ago -
Ripples in a pond travel at a velocity of 3 m/s with one peak
passing a...
asked 3 hours ago -
A man stands on the roof of a building of height 13.0 mm and
throws a...
asked 3 hours ago -
The extent to which assets are financed by borrowed funds and
other liabilities is indicated by:...
asked 4 hours ago -
Explain in detail
Germany is the fifth largest economy
explain what goods and services Germany specializes...
asked 4 hours ago -
The density of platinum is 21.45 g/mL. If a cube of platinum
with a mass of...
asked 4 hours ago -
Accounts Receivable
Sales
A/R Posting
Extended Sales Invoice
Packing Slip
Compare invoice to packing slip 2...
asked 4 hours ago -
Michaella, age 23, is a full-time law student and is claimed by
her parents as a...
asked 4 hours ago -
Why are polymers not typically casted into products?
asked 5 hours ago