REACTION IS WITH PCL3 need help with the final product and mechanism , i know you...
Homework Answers
Add Answer to:
REACTION IS WITH PCL3
need help with the final product and mechanism , i know you...
I know what the final product is, I need help with the reaction mechanism. Please draw and explain reaction mechanism that forms the final product. M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridi...
I know what the final product is, I need help with the reaction
mechanism. Please draw and explain reaction mechanism that forms
the final product.
M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridine К) њег
M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridine
К) њег
I simply need help on these three questions. Thank you Number 3 is asking for the...
I simply need help on these three questions. Thank you
Number 3 is asking for the mechanism but I believe there is a
typo.
I'll have to do number 4 on my own.
Number 5 is asking for a mechanism.
3. Give the reagents/conditions and show the mechanism for the following reaction (15 pts) OH CH3 CH3 4. Dr. Goodchem is making an intermediate. He conducted the reactions below using the conditions given. Explain the rationale behind the methylation of...
I need help answering this problem Give the final product and the mechanism, with all major...
I need help answering this problem
Give the final product and the mechanism, with all major resonance structures, for the following reaction: (upload your answer) NO H-O-H 0: + NO 30: Intermediate Upload Choose a File
What is the major product of the following reaction sequence involving glycolic acid (HOCH2COOH) as the...
What is the major product of the following reaction sequence
involving glycolic acid (HOCH2COOH) as the starting
material?
I understand why Thionyl chloride gets rid of the hydroxyl group
on the carboxylic acid and substitutes it for the chlorine. But,
I have no clue where the extra
carbon came in. I know the answer is D, but I was wondering if it
is possible to show the mechanism as well to help me visualize what
exactly is going on. ?...
I need help on the mechanism of this reaction with the arrows Mechanism Explorer: Sketch and...
I need help on the mechanism
of this reaction with the arrows
Mechanism Explorer: Sketch and Submission Reaction Explorer Help (Intermediate) Reactant (Intermediate) Product Apply Mechanism но- H2C Hint Solution CH3 H3 H3 н,с он 3 remaining step(s) can be solved 2 possible next steps unlocked. Click on [Hint) or [Reset] to cycle through them. H2C Tip: Only add curved arrows in this sketcher
Questions are a continuation of questions 2,3. Thank you for you help! I really need help...
Questions are a continuation of questions 2,3. Thank you for you
help! I really need help with just 3&4.
3.Suppose you wish to perform the reation you wrote in
problem 2 on the other -OH group.How might you prepare the molecule
in order to do so? Suggest appropiate reagents and draw your
expected products.
4. Suppose after your preparation performed in problem
3, the molecule reacts very slowly with HBr. How could you prepare
the -OH group you want to...
5. Give the products of the following reactions. You DO NOT need to show a detailed mechanism but...
5. Give the products of the following reactions. You DO NOT need to show a detailed mechanism but do show ALL reaction intermediates. (30 pts) LiAIH4 G CH3-C-00HE (b) F (c) OH CH3 6. Give the product of the following reactions and in each case give a detailed reaction mechanism by which it is formed. (40 pts, 10 each) pH 4-5 ca. H2S4 HBrJ (c)--/SH NaOH I (d) H CH3 H CH3
5. Give the products of the following reactions....
2. Show the mechanism and product or products for an E2 reaction. (Mechanism 9.5 in your...
2. Show the mechanism and product or products for an E2 reaction. (Mechanism 9.5 in your text walks you through this example). H3CX -CH3 CH CH OH н В a. What is the rate law for an E2 elimination reaction? How does it compare to the rate law for an S2 reaction? b. Do you think that both E2 and S2 reactions will have similar reaction energy diagrams? Why or why not?
I need to do a stepwise mechanism, but I keep ending up with the wrong product, help!
I
need to do a stepwise mechanism, but I keep ending up with the
wrong product, help!
TSOH Bu Bu OH Bu Bry
TSOH Bu Bu OH Bu Bry
I simply need to know what the product formula would be in this reaction. Thank you!!!...
I simply need to know what the product
formula would be in this reaction. Thank you!!!
Experiment 5-Protection of a Carbohydrate: Acetal formation from α-Methylglucopyra noside Reading: Klein 2nd Ed pp 941-943 (acetal formation), 1166-1167 (carbohydrate structure and reactions) Introduction Carbohydrates are a vital part of natural processes: many cellular receptors involve multiple carbohydrates appended to proteins and other biomacromolecules. Synthesizing sugar derivatives is therefore a tremendously important research area in organic chemistry. The problem with sugar chemistry is that...
I know what the final product is, I need help with the reaction
mechanism. Please draw and explain reaction mechanism that forms
the final product.
M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridine К) њег
M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridine
К) њег
I simply need help on these three questions. Thank you
Number 3 is asking for the mechanism but I believe there is a
typo.
I'll have to do number 4 on my own.
Number 5 is asking for a mechanism.
3. Give the reagents/conditions and show the mechanism for the following reaction (15 pts) OH CH3 CH3 4. Dr. Goodchem is making an intermediate. He conducted the reactions below using the conditions given. Explain the rationale behind the methylation of...
I need help answering this problem
Give the final product and the mechanism, with all major resonance structures, for the following reaction: (upload your answer) NO H-O-H 0: + NO 30: Intermediate Upload Choose a File
What is the major product of the following reaction sequence
involving glycolic acid (HOCH2COOH) as the starting
material?
I understand why Thionyl chloride gets rid of the hydroxyl group
on the carboxylic acid and substitutes it for the chlorine. But,
I have no clue where the extra
carbon came in. I know the answer is D, but I was wondering if it
is possible to show the mechanism as well to help me visualize what
exactly is going on. ?...
I need help on the mechanism
of this reaction with the arrows
Mechanism Explorer: Sketch and Submission Reaction Explorer Help (Intermediate) Reactant (Intermediate) Product Apply Mechanism но- H2C Hint Solution CH3 H3 H3 н,с он 3 remaining step(s) can be solved 2 possible next steps unlocked. Click on [Hint) or [Reset] to cycle through them. H2C Tip: Only add curved arrows in this sketcher
Questions are a continuation of questions 2,3. Thank you for you
help! I really need help with just 3&4.
3.Suppose you wish to perform the reation you wrote in
problem 2 on the other -OH group.How might you prepare the molecule
in order to do so? Suggest appropiate reagents and draw your
expected products.
4. Suppose after your preparation performed in problem
3, the molecule reacts very slowly with HBr. How could you prepare
the -OH group you want to...
5. Give the products of the following reactions. You DO NOT need to show a detailed mechanism but do show ALL reaction intermediates. (30 pts) LiAIH4 G CH3-C-00HE (b) F (c) OH CH3 6. Give the product of the following reactions and in each case give a detailed reaction mechanism by which it is formed. (40 pts, 10 each) pH 4-5 ca. H2S4 HBrJ (c)--/SH NaOH I (d) H CH3 H CH3
5. Give the products of the following reactions....
2. Show the mechanism and product or products for an E2 reaction. (Mechanism 9.5 in your text walks you through this example). H3CX -CH3 CH CH OH н В a. What is the rate law for an E2 elimination reaction? How does it compare to the rate law for an S2 reaction? b. Do you think that both E2 and S2 reactions will have similar reaction energy diagrams? Why or why not?
I
need to do a stepwise mechanism, but I keep ending up with the
wrong product, help!
TSOH Bu Bu OH Bu Bry
TSOH Bu Bu OH Bu Bry
I simply need to know what the product
formula would be in this reaction. Thank you!!!
Experiment 5-Protection of a Carbohydrate: Acetal formation from α-Methylglucopyra noside Reading: Klein 2nd Ed pp 941-943 (acetal formation), 1166-1167 (carbohydrate structure and reactions) Introduction Carbohydrates are a vital part of natural processes: many cellular receptors involve multiple carbohydrates appended to proteins and other biomacromolecules. Synthesizing sugar derivatives is therefore a tremendously important research area in organic chemistry. The problem with sugar chemistry is that...
Most questions answered within 3 hours.
-
Write the ionic equations for the first stage of salts
hydrolysis.
Anion, Cation?
Na2S
NiSO4
K2SO4...
asked 1 hour ago -
suppose there is a normally distributed population with a mean of
250 and a standard deviation...
asked 2 hours ago -
Question Three
Suppose you as project manager are using the Waterfall
development methodology on a large...
asked 3 hours ago -
Which statement is not true about welfare in Canada?
A.Benefits typically vary based on one's ability...
asked 3 hours ago -
Please help me with FLOWCHART and UML diagram for class,
thank you!
#include <iostream>
#include <fstream>...
asked 4 hours ago -
3. Describe the “logic circuit” of the Lac operon. Which
proteins are bound or not to...
asked 4 hours ago -
Ayesha’s adjusted gross income is $60,000 in 2019. She donated a
piece of artwork with a...
asked 4 hours ago -
For Dijkstra’s shortest path algorithm:
a. Give the Big-O time for Dijkstra’s shortest path algorithm
and...
asked 4 hours ago -
Phosphorus violates the 'octet rule' in biological molecules,
forming more covalent bonds than expected based on...
asked 4 hours ago -
A 1.3 eV electron has a 10-4 probability of tunneling
through a 2.4 eV potential barrier....
asked 5 hours ago -
What is the one ingredient that is common to being successful
with all stakeholders?
profit
trust...
asked 5 hours ago -
Write an assembly language 32 bit program that reads in lines of
text by a .txt...
asked 5 hours ago