Homework Answers
Add Answer to:
Please explain and right in details
145 1. Write a full, complete mechanism for each of...
please do all and explain sn1 sn2 e1e2 1. Write a full, complete mechanism for each...
please do all and explain sn1 sn2 e1e2
1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
3 (15 marks). Draw a reasonable mechanism that accounts for the formation of the unexpected product...
3 (15 marks). Draw a reasonable mechanism that accounts for the formation of the unexpected product shown below. Use curved arrows to show the movement of electrons and show the structures of all intermediates. Do not draw the structures of transition states. Do not include stereochemistry. Be sure to include formal charges and lone pairs of electrons where appropriate. OH HCI ether
9. a) Write the detailed Sn1 mechanism for the reaction of (S)-3-bromo-3-methylhexane with H20, showing curved...
9. a) Write the detailed Sn1 mechanism for the reaction of (S)-3-bromo-3-methylhexane with H20, showing curved arrows, relevant lone pairs, formal charges, stereochemistry for each step. Include any transition states and/or intermediates, and name the product(s). b) A racemic mixture results from a reaction of the chiral alkylbromide starting material below, and acetate. at hope ܬ Write the complete mechanism for the synthesis. Show the curly arrows, relevant lone pairs and all formal charges for each step. Include any transition...
Provide a mechanism for each of the following reactions. Use arrows to indicate the movement of...
Provide a mechanism for each of the following reactions. Use arrows to indicate the movement of electrons. Be sure to show necessary lone pair electrons and formal charges.
Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all...
Write the complete stepwise mechanism for the
acid catalyzed hydrolysis of the compound shown. Show all
intermediates, indicate with curved arrows the movement of
electrons and show all formal charges and lone pairs of electrons
where relevant. Will rate and comment, thank you in
advance!
8.43 Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions occurring...
8.43 Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions occurring via (a) an S, 2 mechanism and (b) an Swi mechanism. Pay attention to stereochemistry * or Nuct —>?." o Br + NaOH - ? + NaOH - ? н,с fiv) + NaOH ? = > + KBr сн. '+NaOCH, —
i really need help, please help i will rate thanks Write the complete stepwise mechanism for...
i
really need help, please help i will rate thanks
Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all...
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
1. Provide the major product(s) that you would obtain in the following reactions. CH,Br وAIBr 2....
1. Provide the major product(s) that you would obtain in the following reactions. CH,Br وAIBr 2. Provide a mechanism for the following reaction. Use arrows to indicate the movement of electrons. Be sure to show necessary lone pair electrons and formal charges. لملم .هم
To earn full credit and receive feedback, please show all work for all problems. 1. Circle...
To earn full credit and receive feedback, please show all work for all problems. 1. Circle the compound that is the stronger acid. Explain and justify your choice using a combination of words and chemical structures. 2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a...
please do all and explain sn1 sn2 e1e2
1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
3 (15 marks). Draw a reasonable mechanism that accounts for the formation of the unexpected product shown below. Use curved arrows to show the movement of electrons and show the structures of all intermediates. Do not draw the structures of transition states. Do not include stereochemistry. Be sure to include formal charges and lone pairs of electrons where appropriate. OH HCI ether
9. a) Write the detailed Sn1 mechanism for the reaction of (S)-3-bromo-3-methylhexane with H20, showing curved arrows, relevant lone pairs, formal charges, stereochemistry for each step. Include any transition states and/or intermediates, and name the product(s). b) A racemic mixture results from a reaction of the chiral alkylbromide starting material below, and acetate. at hope ܬ Write the complete mechanism for the synthesis. Show the curly arrows, relevant lone pairs and all formal charges for each step. Include any transition...
Provide a mechanism for each of the following reactions. Use arrows to indicate the movement of electrons. Be sure to show necessary lone pair electrons and formal charges.
Write the complete stepwise mechanism for the
acid catalyzed hydrolysis of the compound shown. Show all
intermediates, indicate with curved arrows the movement of
electrons and show all formal charges and lone pairs of electrons
where relevant. Will rate and comment, thank you in
advance!
8.43 Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions occurring via (a) an S, 2 mechanism and (b) an Swi mechanism. Pay attention to stereochemistry * or Nuct —>?." o Br + NaOH - ? + NaOH - ? н,с fiv) + NaOH ? = > + KBr сн. '+NaOCH, —
i
really need help, please help i will rate thanks
Write the complete stepwise mechanism for the acid catalyzed hydrolysis of the compound shown. Show all intermediates, indicate with curved arrows the movement of electrons and show all formal charges and lone pairs of electrons where relevant
2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a proton transfer, be sure to include it (them) in your mechanism. (Remember to start by drawing all ionic compounds as ions/drawing out the structure of all reagents, and drawing in all lone pairs.) HCI 3. Which...
1. Provide the major product(s) that you would obtain in the following reactions. CH,Br وAIBr 2. Provide a mechanism for the following reaction. Use arrows to indicate the movement of electrons. Be sure to show necessary lone pair electrons and formal charges. لملم .هم
To earn full credit and receive feedback, please show all work for all problems. 1. Circle the compound that is the stronger acid. Explain and justify your choice using a combination of words and chemical structures. 2. Provide the complete mechanism (curved arrows) to show how the product is formed. Include all lone pairs, formal charges, curved arrows, intermediates, and products. You do not need to draw the structures of transition states. If there is a carbocation rearrangement and/or a...
Most questions answered within 3 hours.
-
(63
#14)
which of the following statments best describes how chamging
the concentration of the substances...
asked 1 hour ago -
In the following reaction, which element is undergoing
oxidation: Na2SO3 + N2O --> N2 + Na2SO4...
asked 2 hours ago -
Which of the following pairs of ions have the same electron
configuration?
I: Br− and Se2−...
asked 4 hours ago -
The Foremost Composite Materials Company is planning a two-day
sales conference for October 19-20. The conference...
asked 5 hours ago -
3) Illustrate the observed pattern of relatedness of organisms
versus adaptations to specific conditions. This means...
asked 5 hours ago -
In winter a lake has a 0.35 m thick ice layer over 1.10 m of
water....
asked 6 hours ago -
Assuming the following has been encrypted with a Vigenere cipher
below, use the method(s) and assumptions...
asked 6 hours ago -
How would I use switch statements to write a program that will
take an input of...
asked 6 hours ago -
Imagine a reaction in which methane gas combusts at a constant
pressure of 1 atm and...
asked 6 hours ago -
Two parallel wires (each 12 m in length) are separated by a
distance of 0.065 m...
asked 6 hours ago -
Suppose there were three masses at the corner of uniform
equilateral triangle. The masses are m1...
asked 6 hours ago -
Situation: A building that is 618 m above the ground floor. How
many times would a...
asked 6 hours ago