On the SN1 product, where did the hydrogen
go from the OH group in the reactants? Also, why are all the groups
in the carbon in the SN1 product flipped around?
Homework Answers
The answer is given as follows
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On the SN1 product, where did the hydrogen
go from the OH group in the reactants?...
(12) Where in the proof of Theorem 27.11 did we use the fact that G is an Abelian group? Why does...
(12) Where in the proof of Theorem 27.11 did we use the fact that G is an Abelian group? Why doesn't our proof apply to non-Abelian groups? (13) The operation table for D6 the dihedral group of order 12, is given in Table 27.6 FR r rR Table 27.6 Operation table for D6 (a) Find the elements of the set De/Z D6). (b) Write the operation table for the group De/Z(D6) (c) The examples of quotient groups we have seen...
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...
Q1) provide the product for the following reactions, identify as Sn1,Sn2, E1 or E2. Also provide...
Q1) provide the product for the following reactions, identify as Sn1,Sn2, E1 or E2. Also provide the mechanism of the reaction H20 Br NaCN DMSO b). Csi Меон сін C)- KOH ci H d)_ this reaction was run at 100°C and 0.1 M KOH concentration 2) Rank the members of the following groups in order of basicity, nucleophilicity, and leaving group ability. Expain your answers a) H20, OH, CH,CO2- b) Br", ".Fr 3) Predict the effect of the changes given...
1. Why do we want a reaction to go to completion? 2. In general, what are...
1.
Why do we want a reaction to go to completion?
2. In general, what are the most reactive parts of a
molecule?
3. Which TLC plate shows a completed reaction?
SM = Starting Material, RXN = Reaction, P= Product
Why do we want a reaction to go to completion?! Consuming all the starting material means less waste Consuming all the starting material means you don't have to separate the starting material from your product o Consuming all the starting...
5) Iodine is a better leaving group than bromine. But iodine is a better nucleophile than bromine. Why is that? Introdu...
5) Iodine is a better leaving group than bromine. But iodine is
a better nucleophile than bromine. Why is that?
Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via nucleophilic substitution. In this type of reaction, the nucleophile displaces a leaving group from a carbon atom of an organic substrate (here the alcohol once protonated). Both electrons of the new bond to the carbon are provided by the nucleophile while the...
5. All electron-donating groups are activating groups and all are ortho-para directors with the exception of...
5. All electron-donating groups are activating groups and all are ortho-para directors with the exception of substituents, all electron-withdrawing groups are deactivating groups and all are meta directors. A. hydroxyl B. amino C. halogens D. alkoxyl 6. Hydrogen abstraction from the methyl group of methylbenzene (toluene) produces a radical called the radical. A. allylic B. free C. halogen D. benzyllic 7. The stability of benzyllic radicals can be explained by theory. A. resonance B. bond order C. inductive D. molecular...
Exactly what atoms did hydrogen ions fall off in the process of moving from B to C? Please explain the process. R OH OH...
Exactly what atoms did
hydrogen ions fall off in the process of moving from B to C? Please
explain the process.
R OH OH OH OH Он но Он Но H20 но -н R R OGI OGI H OGI +Н,о OGI OH OH -н OH OH A Carbinol pseudo-base : Chalcone B Flavylium cation (red) C :Quinoidial base (blue)
R OH OH OH OH Он но Он Но H20 но -н R R OGI OGI H OGI +Н,о OGI OH...
Canvas What is the major organic product obtained from the following reaction? H OH 2 OH...
Canvas What is the major organic product obtained from the following reaction? H OH 2 OH 1. Os04 2. NaHSO, H20 .st OH OH 3 1 02 3 U Question 54 3.33 pts Question 54 Which functional group below will show a strong peak around 3300 to 3600 cm 1: strong peak at 1700 cm 1, and moderate peak at 1000-1100 cm 1 Carboxylic Acid Carboxylic Ester Amide Alcohol
Draw the neutral organic product that results from the following reaction. Include all hydrogen atoms. Hint:...
Draw the neutral organic product that results from the following
reaction. Include all hydrogen atoms. Hint: we are looking for a
3-carbon product.
(12) Where in the proof of Theorem 27.11 did we use the fact that G is an Abelian group? Why doesn't our proof apply to non-Abelian groups? (13) The operation table for D6 the dihedral group of order 12, is given in Table 27.6 FR r rR Table 27.6 Operation table for D6 (a) Find the elements of the set De/Z D6). (b) Write the operation table for the group De/Z(D6) (c) The examples of quotient groups we have seen...
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...
Q1) provide the product for the following reactions, identify as Sn1,Sn2, E1 or E2. Also provide the mechanism of the reaction H20 Br NaCN DMSO b). Csi Меон сін C)- KOH ci H d)_ this reaction was run at 100°C and 0.1 M KOH concentration 2) Rank the members of the following groups in order of basicity, nucleophilicity, and leaving group ability. Expain your answers a) H20, OH, CH,CO2- b) Br", ".Fr 3) Predict the effect of the changes given...
1.
Why do we want a reaction to go to completion?
2. In general, what are the most reactive parts of a
molecule?
3. Which TLC plate shows a completed reaction?
SM = Starting Material, RXN = Reaction, P= Product
Why do we want a reaction to go to completion?! Consuming all the starting material means less waste Consuming all the starting material means you don't have to separate the starting material from your product o Consuming all the starting...
5) Iodine is a better leaving group than bromine. But iodine is
a better nucleophile than bromine. Why is that?
Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via nucleophilic substitution. In this type of reaction, the nucleophile displaces a leaving group from a carbon atom of an organic substrate (here the alcohol once protonated). Both electrons of the new bond to the carbon are provided by the nucleophile while the...
5. All electron-donating groups are activating groups and all are ortho-para directors with the exception of substituents, all electron-withdrawing groups are deactivating groups and all are meta directors. A. hydroxyl B. amino C. halogens D. alkoxyl 6. Hydrogen abstraction from the methyl group of methylbenzene (toluene) produces a radical called the radical. A. allylic B. free C. halogen D. benzyllic 7. The stability of benzyllic radicals can be explained by theory. A. resonance B. bond order C. inductive D. molecular...
Exactly what atoms did
hydrogen ions fall off in the process of moving from B to C? Please
explain the process.
R OH OH OH OH Он но Он Но H20 но -н R R OGI OGI H OGI +Н,о OGI OH OH -н OH OH A Carbinol pseudo-base : Chalcone B Flavylium cation (red) C :Quinoidial base (blue)
R OH OH OH OH Он но Он Но H20 но -н R R OGI OGI H OGI +Н,о OGI OH...
Canvas What is the major organic product obtained from the following reaction? H OH 2 OH 1. Os04 2. NaHSO, H20 .st OH OH 3 1 02 3 U Question 54 3.33 pts Question 54 Which functional group below will show a strong peak around 3300 to 3600 cm 1: strong peak at 1700 cm 1, and moderate peak at 1000-1100 cm 1 Carboxylic Acid Carboxylic Ester Amide Alcohol
Draw the neutral organic product that results from the following
reaction. Include all hydrogen atoms. Hint: we are looking for a
3-carbon product.
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