NEED HELP WITH ORAGNIC ASAP! NEED STEP-BY-STEP
REASONING AND EXPLAIN EVERYTHING.MUST SHOW ALL WORK AND STEPS
PLEASE AND SHOW STEREOCHEMISTRY FOR EACH REACTION!!! (PLEASE DONT
REPOST OLD ANSWERS) The (-------) lines indicate unspecified
steriochemistry please identify those!!! And show all intermediate
via arrow pushing.PLEASE DO 2A AND 2B!
Homework Answers
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NEED HELP WITH ORAGNIC ASAP! NEED STEP-BY-STEP
REASONING AND EXPLAIN EVERYTHING.MUST SHOW ALL WORK AND STEPS...
Need help with all 4 of these synthesis reactions. Br in first question and wants to...
Need help with all 4 of these synthesis
reactions.
Br in first question and wants to see all arrow pushing,
intermediates and products.
Last three just want the numbered reagents and the
intermediate products after each step. No arrow pushing.
Homework #1 Name: 1. Explain with a mechanism the observation of the given products. (Hint: You will need the full reaction mechonism including all intermediates and reogents, Show the proper use of electron pushing arrows.) HBr 2. Propose an efficient...
20. Design a synthesis to perform the following transformations. Show all reagents and synthetic intermediates. Abo...
20. Design a synthesis to perform the following transformations. Show all reagents and synthetic intermediates. Above each arrow is the number of steps each synthesis can be performed in, but you can use as many steps as you need. che sia ke - x ОН ОН when ich OMe 3 Meo
please show all steps and most important, please explain what's going on here. I'm most confused...
please show all steps and most important, please explain
what's going on here. I'm most confused about the last step, but my
entire understanding of this problem could use work. thank you in
advance
15) (7 points) Draw the intermediates (A and B) and the product (C) of the cyclopentene using the following reagents (no need to draw the mechanism). For each molecule (A, B and C), draw the stereochemistry of the 2 chiral centers that were formed A C...
Show the most efficient synthesis of the product from the starting material. Show all reagents your...
Show the most efficient synthesis of the product from the starting material. Show all reagents your need over each arrow, and draw all products and intermediates (do not combine steps). You do not need to show the mechanism for any steps. Show all molecules synthesized along the way, and pay attention to stereochemistry. If a racemic mixture is produced in any step, show both products formed. If you make a mixture of regioisomers in any of the steps, place a...
Please explain with steps for each problem...and label Write the step by step reaction mechanisms of...
Please explain with steps for each problem...and label
Write the step by step reaction mechanisms of the following reactions. Show all the reaction intermediates. Use arrows, charges, and work up steps. There are two steps.
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all...
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH BONUS: Please provide the arrow pushing mechanism of this reaction. Be sure to show a charges and stereochemistry where needed. To receive full credit, what is the name of this reaction? (4) NaOE HOE Br
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synth...
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synthetic transformations may be achieved. Give reagents and conditions for each step. Include all synthetic intermediates compounds produced during the course of multi-step synthesis). NOTE: You may not use HOC OH 1. For each of the following questions, provide the missing reagents that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic...
show all of steps required to achieve the transformation shown below. For each step include all...
show all of steps required to achieve the transformation shown below. For each step include all applicable starting material(s), solvent(s), reagents or catalysts required. You should show each step as a balanced reaction, but you do not need to draw full mechanisms. [3.0 Marks 0
can you please explain each step and why its occurring!! can you explain why each step...
can you please explain each step and why its occurring!!
can you explain why each step is occuring as well. please! 3. Show how the following conversions could be carried out in three or fewer steps. Provide structures for each intermediate, which would be isolated and indicate reagents and conditions for each step. Pay close attention to stereochemistry. CH3 ...CH • ? for • 208 OCH2CH3
please help asap Question 3 (36 pts.) For each of the following reactions: a) Provide the...
please help asap
Question 3 (36 pts.) For each of the following reactions: a) Provide the missing major organic product. Pay attention to stereochemistry unless directed otherwise and identify any racemic mixtures using the (1) symbol. c) Assign each reaction as OXIDATION or REDUCTION as appropriate NaBH, ETOH 1. Excess LIAIH 2. H2O nyomas La Na, Cr20;/H,SO/H, Excess PCC/CH_C12 OH Question 4 (22 pts.). Synthesize the target) molecule on the right from the starting molecule the left Give reagents and...
Need help with all 4 of these synthesis
reactions.
Br in first question and wants to see all arrow pushing,
intermediates and products.
Last three just want the numbered reagents and the
intermediate products after each step. No arrow pushing.
Homework #1 Name: 1. Explain with a mechanism the observation of the given products. (Hint: You will need the full reaction mechonism including all intermediates and reogents, Show the proper use of electron pushing arrows.) HBr 2. Propose an efficient...
20. Design a synthesis to perform the following transformations. Show all reagents and synthetic intermediates. Above each arrow is the number of steps each synthesis can be performed in, but you can use as many steps as you need. che sia ke - x ОН ОН when ich OMe 3 Meo
please show all steps and most important, please explain
what's going on here. I'm most confused about the last step, but my
entire understanding of this problem could use work. thank you in
advance
15) (7 points) Draw the intermediates (A and B) and the product (C) of the cyclopentene using the following reagents (no need to draw the mechanism). For each molecule (A, B and C), draw the stereochemistry of the 2 chiral centers that were formed A C...
Show the most efficient synthesis of the product from the starting material. Show all reagents your need over each arrow, and draw all products and intermediates (do not combine steps). You do not need to show the mechanism for any steps. Show all molecules synthesized along the way, and pay attention to stereochemistry. If a racemic mixture is produced in any step, show both products formed. If you make a mixture of regioisomers in any of the steps, place a...
Please explain with steps for each problem...and label
Write the step by step reaction mechanisms of the following reactions. Show all the reaction intermediates. Use arrows, charges, and work up steps. There are two steps.
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH BONUS: Please provide the arrow pushing mechanism of this reaction. Be sure to show a charges and stereochemistry where needed. To receive full credit, what is the name of this reaction? (4) NaOE HOE Br
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synthetic transformations may be achieved. Give reagents and conditions for each step. Include all synthetic intermediates compounds produced during the course of multi-step synthesis). NOTE: You may not use HOC OH 1. For each of the following questions, provide the missing reagents that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic...
show all of steps required to achieve the transformation shown below. For each step include all applicable starting material(s), solvent(s), reagents or catalysts required. You should show each step as a balanced reaction, but you do not need to draw full mechanisms. [3.0 Marks 0
can you please explain each step and why its occurring!!
can you explain why each step is occuring as well. please! 3. Show how the following conversions could be carried out in three or fewer steps. Provide structures for each intermediate, which would be isolated and indicate reagents and conditions for each step. Pay close attention to stereochemistry. CH3 ...CH • ? for • 208 OCH2CH3
please help asap
Question 3 (36 pts.) For each of the following reactions: a) Provide the missing major organic product. Pay attention to stereochemistry unless directed otherwise and identify any racemic mixtures using the (1) symbol. c) Assign each reaction as OXIDATION or REDUCTION as appropriate NaBH, ETOH 1. Excess LIAIH 2. H2O nyomas La Na, Cr20;/H,SO/H, Excess PCC/CH_C12 OH Question 4 (22 pts.). Synthesize the target) molecule on the right from the starting molecule the left Give reagents and...
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