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Complete the following equations (assuming that the reactions occur via a bromonium ion). There is no need to writ...
3. Assign Rors configuration to the following molecules: - Br Br F Br -CH CH.CH H...
3. Assign Rors configuration to the following molecules: - Br Br F Br -CH CH.CH H CH2CHE CH2CH CH, CH -CH, OH H -CH=CH2 H3C 7 Сн, HI CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds u 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) BE CHO -Br (or CI) Br
Please answer all three if possible but mainly number 5 Br SCHLECH, 3. Assign R or...
Please answer all three if possible but mainly number 5
Br SCHLECH, 3. Assign R or Sconfiguration to the following molecules: Br F H. I H Br CH F F I . CH2CH3 CH2CH3 CH3CH -CH3 OH CH=CH2 H3C Сн, H "CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers c. identical d. Meso Compounds GH 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate...
How to solve alkene and alkyne reactions - Merdanym i Act antalyzod Hrdian ca Come Lazarmistry...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
*Ignore the structures drawn in pencil. The purple lines indicate that they are incorrect. 23. As 5 points. Complete 10 of the 15 following reactions by providing the missing information: reac...
*Ignore the structures drawn in pencil. The purple lines
indicate that they are incorrect.
23. As 5 points. Complete 10 of the 15 following reactions by providing the missing information: reactants products or reagents and conditions. When predicting products, you must include all products that will most likely form in an appreciable amount. When more than one product is likely, label the major and minor products. (Watch out for rearrangements). Where appropriate, indicate stereochemistry, as well as whether or not...
B (Complete the following reactions by putting the structure of the missing compound or reagent in...
B (Complete the following reactions by putting the structure of the missing compound or reagent in the given box. Show stereochemistry clearly where applicable Bopas) 1. KMnO4 (1 2. + H₂O Na BH 3. 4. o CEC-chy Ly og 22, Acetic acid +Bel 6. Intermediate product BH THE the 7. ON peroxide a 8. + H Br hu 9. 10. OCCH), t.com heat CL 11. NOL Aceton B (LU) Using the following analytical results, determine the molecular structure of compounds...
19-26 thanks! 19-29* PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of...
19-26 thanks!
19-29*
PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of 2,3-butanediol as you can. First, attach two carbons with a single bond. To each carbon add one carbon, one hydrogen, and one oxygen. To complete the structure, Ti the remaining hydrogen atoms. Remember, a model is not different if it is completely superimposable on one already constructed! 13. How many stereochemically different models are possible for 2,3-butanediol? 14. What characteristic does one of these...
How to properly solve these elimination and addition reactions Elimination and Addition reactions Purpose: Fi...
How to properly solve these elimination and addition
reactions
Elimination and Addition reactions Purpose: Figuring out the ways that molecules react is the province of the mechanistic chemist. By understanding the mechanisms of reactions, the chemist can manipulate the experimental variables to favor one product over another. This element of control is the province of the synthetic organic chemist. This Workshop continues to explore how we know how molecules react and how this knowledge leads to control of the products....
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
4.81,4.82 Chapter Review 177 481 Are the following compounds structural isomers, cis-trans isomers, or enantiomers? 4.82...
4.81,4.82
Chapter Review 177 481 Are the following compounds structural isomers, cis-trans isomers, or enantiomers? 4.82 Draw the enantiomer of each of the following com- pounds. If the compound is not chiral, state that fact. a. H Η and b. HO Find Br" CH, MF HC Br b. Br но Br. OH w and b. H H-C-H HH H-C-C-C- H C H,CH(CH), c. Che Problems 4.83 Cartat omega-3 fatty acids can be found only in animal sources, such as fatty...
3. Assign Rors configuration to the following molecules: - Br Br F Br -CH CH.CH H CH2CHE CH2CH CH, CH -CH, OH H -CH=CH2 H3C 7 Сн, HI CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds u 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) BE CHO -Br (or CI) Br
Please answer all three if possible but mainly number 5
Br SCHLECH, 3. Assign R or Sconfiguration to the following molecules: Br F H. I H Br CH F F I . CH2CH3 CH2CH3 CH3CH -CH3 OH CH=CH2 H3C Сн, H "CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers c. identical d. Meso Compounds GH 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
*Ignore the structures drawn in pencil. The purple lines
indicate that they are incorrect.
23. As 5 points. Complete 10 of the 15 following reactions by providing the missing information: reactants products or reagents and conditions. When predicting products, you must include all products that will most likely form in an appreciable amount. When more than one product is likely, label the major and minor products. (Watch out for rearrangements). Where appropriate, indicate stereochemistry, as well as whether or not...
B (Complete the following reactions by putting the structure of the missing compound or reagent in the given box. Show stereochemistry clearly where applicable Bopas) 1. KMnO4 (1 2. + H₂O Na BH 3. 4. o CEC-chy Ly og 22, Acetic acid +Bel 6. Intermediate product BH THE the 7. ON peroxide a 8. + H Br hu 9. 10. OCCH), t.com heat CL 11. NOL Aceton B (LU) Using the following analytical results, determine the molecular structure of compounds...
19-26 thanks!
19-29*
PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of 2,3-butanediol as you can. First, attach two carbons with a single bond. To each carbon add one carbon, one hydrogen, and one oxygen. To complete the structure, Ti the remaining hydrogen atoms. Remember, a model is not different if it is completely superimposable on one already constructed! 13. How many stereochemically different models are possible for 2,3-butanediol? 14. What characteristic does one of these...
How to properly solve these elimination and addition
reactions
Elimination and Addition reactions Purpose: Figuring out the ways that molecules react is the province of the mechanistic chemist. By understanding the mechanisms of reactions, the chemist can manipulate the experimental variables to favor one product over another. This element of control is the province of the synthetic organic chemist. This Workshop continues to explore how we know how molecules react and how this knowledge leads to control of the products....
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
4.81,4.82
Chapter Review 177 481 Are the following compounds structural isomers, cis-trans isomers, or enantiomers? 4.82 Draw the enantiomer of each of the following com- pounds. If the compound is not chiral, state that fact. a. H Η and b. HO Find Br" CH, MF HC Br b. Br но Br. OH w and b. H H-C-H HH H-C-C-C- H C H,CH(CH), c. Che Problems 4.83 Cartat omega-3 fatty acids can be found only in animal sources, such as fatty...
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