Homework Answers
Add Answer to:
please show all the arrows
ethylamine does not provide any product (1). However, when Ill is...
clearer images For questions 1 - 5. predict the major organic products for the following transformations....
clearer images
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. OH 1. a) Croy, H,SO,,H,O (Jones reagent) b) workup 2. a) HCI (cat.), CH, OH b) workup Q2 1. a) Croy, pyridine, HCl, solvent (PCC) b) workup 2. a) HCI (cat.), CH, OH b) workup a) NaOH, solvent,...
please help solve For questions 1 - 5. predict the major organic products for the following...
please help solve
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. CHO a) Nah, solvent b) workup a) LDA, solvent b) CH, Br, solvent c) workup a) Nah, solvent b) CH, Br, solvent c) workup CHO a) NaOH,H,O, HEAT b) workup a)excess NaOCH, CH, OH b)1,4-dibromobutane, solvent c)...
please solve these questions thank you so much For questions 1-9, select the reaction conditions (A-1)...
please solve these questions
thank you so much
For questions 1-9, select the reaction conditions (A-1) which would create the major organic product(s) in the number of steps permitted in each box. a) H,50, (cat.), NH, b) workup a) Cro ,H, SOX, H,0 (Jones Reagent) b) workup a) H.SO(cat.), CH,OH b) workup a) H,50,(cat.),(CH), NH b) workup a) NaBH, CH,OH b) H20-workup a) Croy, pyridine, HCl, solvent (PCC) b) workup a) H, 50, (cat.), CH,CH,OH b) workup a)H,SO, (cat.), CH...
please help solve this Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanis...
please help solve this
Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanism which relates the starting materials to the products. Messy or incoherent answers will result in reduced or zero credit. Clearly cross out or remove anything you do not wish graded. All protonations/deprotonations must be explicitly shown; use of "proton transfer or P.T." is not permitted, and will receive zero credit if used in error. Clearly indicate formal charges if applicable. a)H,50 (cat.),...
For questions 1-4, provide the missing reactant(s), reagent(s), or major organic product(s) of each reaction. Only...
For questions 1-4, provide the missing reactant(s), reagent(s), or major organic product(s) of each reaction. Only one type of species is missing for each reaction. If you are providing reactant(8) or product(s), be sure to indicate stereochemistry if it is relevant. If you are providing reagents and more than one step is required, be sure to number each step. 1. EtMgBr 2.H20 NH [H] 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you...
please help in all sections!! What would be the product of the following reaction? H 1....
please help in all sections!!
What would be the product of the following reaction? H 1. LAIH 2. H₂O OH OH What would be the product of the following reaction? H NaBH,/CH3OH OH Which of the following compounds is least reactive towards a nucleophilic addition reaction? Both I and IV Predict the product for the following reaction. CH3CH2NH2 H2SO4 CH-CH2NH2 ΝΗ, HO NH HẠN Which of the following compounds can be classified as a hemiacetal? 0 он Provide the structure...
please solve all 8. Provide an efficient multi-step synthesis of 2 starting with 1. In your...
please solve all
8. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents used for each step by writing them over the arrow leading to cach of the specified products. At some point in your synthesis you must utilize the chemical(s) specified over the arrows. opo maeneo l 5. Draw the major product for each of the following reactions or reaction sequences. Show stereochemistry where appropriate. Assume aqueous workup. 1) Fe, HCI...
Provide the missing reagent or major organic product from the following reaction sequence. Take note of...
Provide the missing reagent or major organic product from the following reaction sequence. Take note of the direction of the arrows. Write only the corresponding letters or numbers in the space provided. If the reagent or product is not available then write NONE. Assume aqueous workup is applied at the end of the reaction except for deprotonation reactions. Br 2 PhMgBr х Dess Martin (CH3)2Culi Y REAGENT BANK A. PBrz, Br2 D. NaOEt, EtOH G. CH3OH B. HBr, Br2 E....
Do all work on this paper. 1. The compound below on the left has a much...
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
please help in all sections asap!! Predict the product for the following reaction sequence: MgBr PCO...
please help in all sections asap!!
Predict the product for the following reaction sequence: MgBr PCO CHCE etler Predict the product for the following reaction, Predict the product for the following reaction. excess CH3OH H2SO4 H3CO OCHз Но осна ОСН3 Which one of the following compounds will yield 1-hexanol when treated with butylmagnesium bromide followed by acid workup? 1-hexanol formaldehyde acetaldehyde odrane hexanal Provide the reagents necessary to carry out the following conversion. 1. H20/ H2SO4 2. PCC/CH2Cl2 PCC/ CH2Cl2...
clearer images
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. OH 1. a) Croy, H,SO,,H,O (Jones reagent) b) workup 2. a) HCI (cat.), CH, OH b) workup Q2 1. a) Croy, pyridine, HCl, solvent (PCC) b) workup 2. a) HCI (cat.), CH, OH b) workup a) NaOH, solvent,...
please help solve
For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. CHO a) Nah, solvent b) workup a) LDA, solvent b) CH, Br, solvent c) workup a) Nah, solvent b) CH, Br, solvent c) workup CHO a) NaOH,H,O, HEAT b) workup a)excess NaOCH, CH, OH b)1,4-dibromobutane, solvent c)...
please solve these questions
thank you so much
For questions 1-9, select the reaction conditions (A-1) which would create the major organic product(s) in the number of steps permitted in each box. a) H,50, (cat.), NH, b) workup a) Cro ,H, SOX, H,0 (Jones Reagent) b) workup a) H.SO(cat.), CH,OH b) workup a) H,50,(cat.),(CH), NH b) workup a) NaBH, CH,OH b) H20-workup a) Croy, pyridine, HCl, solvent (PCC) b) workup a) H, 50, (cat.), CH,CH,OH b) workup a)H,SO, (cat.), CH...
please help solve this
Question 10. Using arrows to indicate the flow of electrons, provide a step-by-step mechanism which relates the starting materials to the products. Messy or incoherent answers will result in reduced or zero credit. Clearly cross out or remove anything you do not wish graded. All protonations/deprotonations must be explicitly shown; use of "proton transfer or P.T." is not permitted, and will receive zero credit if used in error. Clearly indicate formal charges if applicable. a)H,50 (cat.),...
For questions 1-4, provide the missing reactant(s), reagent(s), or major organic product(s) of each reaction. Only one type of species is missing for each reaction. If you are providing reactant(8) or product(s), be sure to indicate stereochemistry if it is relevant. If you are providing reagents and more than one step is required, be sure to number each step. 1. EtMgBr 2.H20 NH [H] 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you...
please help in all sections!!
What would be the product of the following reaction? H 1. LAIH 2. H₂O OH OH What would be the product of the following reaction? H NaBH,/CH3OH OH Which of the following compounds is least reactive towards a nucleophilic addition reaction? Both I and IV Predict the product for the following reaction. CH3CH2NH2 H2SO4 CH-CH2NH2 ΝΗ, HO NH HẠN Which of the following compounds can be classified as a hemiacetal? 0 он Provide the structure...
please solve all
8. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents used for each step by writing them over the arrow leading to cach of the specified products. At some point in your synthesis you must utilize the chemical(s) specified over the arrows. opo maeneo l 5. Draw the major product for each of the following reactions or reaction sequences. Show stereochemistry where appropriate. Assume aqueous workup. 1) Fe, HCI...
Provide the missing reagent or major organic product from the following reaction sequence. Take note of the direction of the arrows. Write only the corresponding letters or numbers in the space provided. If the reagent or product is not available then write NONE. Assume aqueous workup is applied at the end of the reaction except for deprotonation reactions. Br 2 PhMgBr х Dess Martin (CH3)2Culi Y REAGENT BANK A. PBrz, Br2 D. NaOEt, EtOH G. CH3OH B. HBr, Br2 E....
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
please help in all sections asap!!
Predict the product for the following reaction sequence: MgBr PCO CHCE etler Predict the product for the following reaction, Predict the product for the following reaction. excess CH3OH H2SO4 H3CO OCHз Но осна ОСН3 Which one of the following compounds will yield 1-hexanol when treated with butylmagnesium bromide followed by acid workup? 1-hexanol formaldehyde acetaldehyde odrane hexanal Provide the reagents necessary to carry out the following conversion. 1. H20/ H2SO4 2. PCC/CH2Cl2 PCC/ CH2Cl2...
Most questions answered within 3 hours.
-
A sample of C3H8 has 1.60×1024 H atoms.
How many carbon atoms does the sample contain?...
asked 2 minutes ago -
Discuss the sales orders process module(s) in the Enterprise
Resource Planning system. How does it contribute...
asked 5 minutes ago -
The position in an object as a function of time is given as ?
(?) =...
asked 5 minutes ago -
Design a class for python named PersonData with the following
member variables:
lastName
firstName
address
city...
asked 19 minutes ago -
How does use of the risk/need/responsivity model impact
effective rehabilitation services?
asked 23 minutes ago -
Your rich uncle has just given you a high school graduation
present of $900,000. The present,...
asked 25 minutes ago -
1=Write a program in C to get 16-bit data from Port-D and send
it to ports...
asked 24 minutes ago -
Calculate Ecell for the following reaction and conditions: 0.50
M Br2 (aq), 0.10 M Pb+2 (aq),...
asked 45 minutes ago -
There can be more than one correct answer.
Hypophysiotropic hormones:
A. released by the hypothalamus
B....
asked 50 minutes ago -
Scott Ruskin is the CEO of Decatur Materials. The company has
been struggling for the last...
asked 48 minutes ago -
If you were conducting a study involving twins regarding
genetics and/or upbringing, which would you use?...
asked 1 hour ago -
Part 1- Inventory: You own a toy company and
you are producing wooden rocking horses. Assume...
asked 1 hour ago