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7 Complete the following reaction by giving Products and idenifing...
*PLEASE provide the right answer with detailed steps and explanation and then I will give you...
*PLEASE provide the right answer with detailed steps and
explanation and then I will give you a thumbs up (if it's
right).
A 18.6 ml solution of 0.100 mol -- HOCI is titrated using 0.150 mol (NaOH. What is the pH of the solution after 5.89 mL of the NaOH solution is added? Express your answer to 2 decimal places. You have 5 attempts at this question. Remember you can find KA and/or Kg values in your textbook chapter 15.
Show the complete detailed mechanism for the following reaction. Provide all possible products and indicate specific...
Show the complete detailed mechanism for the following
reaction. Provide all possible products and indicate specific
stereochemistry or regio-chemistry if appropriate
Cl B. NaOH. H,O → 2 350°C products
please provide a full explanation on how you got the answers and please answer all of...
please provide a full explanation on how you got the answers and
please answer all of the questions!
1) Name the following compounds: (8 pts) Br 1a) 1b) 2) Draw the major product and write a mechanism for the reaction. (12 pts) Br NaOET EtOH, 60 °C 3) Draw the major product and write a mechanism for the reaction. (10 pts) HBr, 0°C Draw the major product of the reaction shown below. Propose a detailed mechanism for the reaction. HBr...
2. For the Su2 reaction depicted below, (a) please form all possible products and (b) draw...
2. For the Su2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains the formation of these products. (5 pts) Br OO. к :осн,сH, CH3 THF
Please show complete arrow pushing mechanism for the following reaction. The answer had three products and...
Please show complete arrow pushing mechanism for the following
reaction. The answer had three products and I am not sure why.
Please answer all parts for good rating! 2) Predict the products and provide the complete arrow-pushing...
Please answer all parts for good rating!
2) Predict the products and provide the complete arrow-pushing mechanism for the reaction below. viere —
1. Please provide the major products of Friday's reaction: n-Bu NBP NaOH, H2O снэ CH3 2....
1. Please provide the major products of Friday's reaction: n-Bu NBP NaOH, H2O снэ CH3 2. Please provide an arrow-pushing mechanism for the above reaction - Williamson ether synthesis. (You do not have to account for the n-Bu-NBr in the mechanism)
please answer i,ii,iii,iv,v Predict the major product(s) of the following reaction, giving regiochemical and/or stereochemical details...
please
answer i,ii,iii,iv,v
Predict the major product(s) of the following reaction, giving regiochemical and/or stereochemical details as relevant. (6 MARKS) q Bry, H0 ? ANSWER: (ii) Predict the product(s) of the oxidation of 2,3,4-trimethyl-1,5-heptadiene with hot, alkaline KMnO4 followed by acidic work up. (6 MARKS) (iii) Complete the following reaction sequence, giving structures for compounds C and D (Na2CO3 just acts as a base!): CH,SOCI CH,OH Na2CO3 D DMF (6 MARKS) D (iv) Supply the missing structures A and B....
I need the mechanism please. IV. Provide a complete stepwise mechanism for the following reaction sequence,...
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
***Please help answer the questions and provide explanation*** 4) Provide the reagents needed to complete the...
***Please help answer the questions and provide
explanation***
4) Provide the reagents needed to complete the following series of steps: 3) 2) 5) 5) In homework #4, you were asked why two equivalents of methylmagnesium bromide were required for this transformation: 1) CH3MgBr (2 eq.) 2)H30. OH Now, based on your knowledge of protecting groups, provide reagents needed to complete this same transformation. 1) 2) 3) (Note: step 3 accomplishes two things in the same step). 6) Predict the products...
*PLEASE provide the right answer with detailed steps and
explanation and then I will give you a thumbs up (if it's
right).
A 18.6 ml solution of 0.100 mol -- HOCI is titrated using 0.150 mol (NaOH. What is the pH of the solution after 5.89 mL of the NaOH solution is added? Express your answer to 2 decimal places. You have 5 attempts at this question. Remember you can find KA and/or Kg values in your textbook chapter 15.
Show the complete detailed mechanism for the following
reaction. Provide all possible products and indicate specific
stereochemistry or regio-chemistry if appropriate
Cl B. NaOH. H,O → 2 350°C products
please provide a full explanation on how you got the answers and
please answer all of the questions!
1) Name the following compounds: (8 pts) Br 1a) 1b) 2) Draw the major product and write a mechanism for the reaction. (12 pts) Br NaOET EtOH, 60 °C 3) Draw the major product and write a mechanism for the reaction. (10 pts) HBr, 0°C Draw the major product of the reaction shown below. Propose a detailed mechanism for the reaction. HBr...
2. For the Su2 reaction depicted below, (a) please form all possible products and (b) draw the mechanism using curved arrow notation that explains the formation of these products. (5 pts) Br OO. к :осн,сH, CH3 THF
Please show complete arrow pushing mechanism for the following
reaction. The answer had three products and I am not sure why.
Please answer all parts for good rating!
2) Predict the products and provide the complete arrow-pushing mechanism for the reaction below. viere —
1. Please provide the major products of Friday's reaction: n-Bu NBP NaOH, H2O снэ CH3 2. Please provide an arrow-pushing mechanism for the above reaction - Williamson ether synthesis. (You do not have to account for the n-Bu-NBr in the mechanism)
please
answer i,ii,iii,iv,v
Predict the major product(s) of the following reaction, giving regiochemical and/or stereochemical details as relevant. (6 MARKS) q Bry, H0 ? ANSWER: (ii) Predict the product(s) of the oxidation of 2,3,4-trimethyl-1,5-heptadiene with hot, alkaline KMnO4 followed by acidic work up. (6 MARKS) (iii) Complete the following reaction sequence, giving structures for compounds C and D (Na2CO3 just acts as a base!): CH,SOCI CH,OH Na2CO3 D DMF (6 MARKS) D (iv) Supply the missing structures A and B....
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
***Please help answer the questions and provide
explanation***
4) Provide the reagents needed to complete the following series of steps: 3) 2) 5) 5) In homework #4, you were asked why two equivalents of methylmagnesium bromide were required for this transformation: 1) CH3MgBr (2 eq.) 2)H30. OH Now, based on your knowledge of protecting groups, provide reagents needed to complete this same transformation. 1) 2) 3) (Note: step 3 accomplishes two things in the same step). 6) Predict the products...
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