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1. Consider the following reaction below to answer the following questions. As indicated by the carbon...
What is the major product of the following reaction? Hy(excess) Lindlar's cat. A B D Ос...
What is the major product of the following reaction? Hy(excess) Lindlar's cat. A B D Ос B A D What is the major product of the following reaction? Cl2 Н,0 НО СІ. A \ Он С В с D CI CI ОН ОН Ов ОА D с What is the major product of the following reaction? CH3 нс Н сH,CH, NaNH2 DMSO Br А В CH3 CHCH3 9 CH3 с CH,CH H4C. D нс CH2CH3 CH3 "NH, нс Сн HECH...
can you double check these answers? 11. Consider the Grignard reaction below to answer the following...
can you double check these answers?
11. Consider the Grignard reaction below to answer the following question(s). HO muchopnice electronice 3.CH Mg ch нс CH, 2 Hot : A the alcohol product can be classified as a .3 alcanot The nucleophile in this reaction is: 1' alcohol 2' alcohol 3' alcohol 4 alcohol 12. To answer the following question(s), consider the reaction below: OH POCH Pyridine CH CH3 Draw arrows which account for the complete stepwise mechanism for this reaction....
Assign R, S configurations to each indicated chirality center in the molecules below. B. COOH A....
Assign R, S configurations to each indicated chirality center in the molecules below. B. COOH A. OH HOW -H CHANH HNCH HO norepinephrine alamine HOC / OH CH3 не HC HÓ COH tartaric acid CH2 dihadrocarpone The configuration of this carbon atom (A) is · (2 pts.) The configuration of this carbon atom (B) is _ . (2 pts.) The configuration of this carbon atom (C) is . (2 pts.) . The configuration of this carbon atom (D) is __....
star each asymmetric carbon atom in the following examples & determine whether it has the R...
star each asymmetric carbon atom in the following examples
& determine whether it has the R or S configuration
PROBLEM 5-6 Star () each asymmetric carbon atom in the following examples, and determine whether it has the (R) or (S) configuration. сн, Н Н H CH, (c) H. (a) (b) Br но с, CH сH CH, CH,CH НС н н CH, Н (d) (e) (D Н Н Cl H Cl Cl СНO (g) (h) ("i) CH CH, (CH,O),CH CH(CH), D...
could someone answer these for me please 1. Use numbers to indicate which compound will react...
could someone answer these for me please
1. Use numbers to indicate which compound will react the fastest by the Ss2 med these alcohols with Nal in acetone. With 1 being the fastest and 4 being the slowest (10 ne lastest by the S2 mechanism for нс , H₂C нсон, Br H₂C * now the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CHE conc. HBr CH, HCM Syl condition...
7. Refer to Exhibit 5-3. The configuration of this carbon atom (E) 15 Exhibit 5-4 Consider...
7. Refer to Exhibit 5-3. The configuration of this carbon atom (E) 15 Exhibit 5-4 Consider the structure of streptimidone to answer the following question(s): OH OH нс н stopuklone ĄCH 8. Refer to Exhibit 5-4. Assign Ror Sconfiguration to each chirality center indicated in streptimidone. 9. Refer to Exhibit 5-4. Will streptimidone have a meso stereoisomer? Explain your answer. Exhibit 5-5 Label each pair of stereoisomers below as: a. enantiomers b. diastereomers c. identical Place the letter of the...
For each of the structures below draw the alcohol that would be predominatly formed from the...
For
each of the structures below draw the alcohol that would be
predominatly formed from the hydration (an addition reaction) of
the double bond.
For each of the structures below draw the alcohol that would be predominantly formed from the hydration (an addition reaction) of the double bond. 10. H3C-CH==CH2 + H2O 11. + H2O - H₂CC=CH₂ + H₂O нс CH2 + H₂O CH3 3 + H₂O
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What...
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What is the product of this bromination reaction? H2C-CH=CH-CH2-CH2-CH3 + Br2 3. What is the product of this oxidation reaction? OH H3C-CH-CH-CHg 10 Сн, 4. Consider the esterification reaction reaction below: H, SO H3C-CH2-CH2-CH2-C-OH + H2C-CH2-OH What organic compound is the reactant on the left? What organic compound is the reactant on the right? Draw the product of the reaction. What type of organic compound...
Predict the products formed in the following reactions. Predict the product(s) formed in the following reactions....
Predict the products formed in the following reactions.
Predict the product(s) formed in the following reactions. If there is no reaction, write “No Rxn" as the answer for the major product and leave the minor product box blank. If there is no minor product in the reaction, then leave the minor product box blank. If there are multiple products, make sure the products are in the appropriate box. (24 points, 4 points each) Note: Do not over complicate some questions...
Assign R, S configurations to each indicated che e se A. OH! HO TTCH NH, merupp hale HOC / OH H HO HC COZH acid tar...
Assign R, S configurations to each indicated che e se A. OH! HO TTCH NH, merupp hale HOC / OH H HO HC COZH acid tarber CH, 1. The configuration of this carbon atom (A) is 2. The configuration of this carbon atom (B) is 3. The configuration of this carbon atom (E) is Consider the structure of streptimidone to answer the following question(s). OH OH strep timidone H3C H 4. Assign R or S configuration to each chirality center...
What is the major product of the following reaction? Hy(excess) Lindlar's cat. A B D Ос B A D What is the major product of the following reaction? Cl2 Н,0 НО СІ. A \ Он С В с D CI CI ОН ОН Ов ОА D с What is the major product of the following reaction? CH3 нс Н сH,CH, NaNH2 DMSO Br А В CH3 CHCH3 9 CH3 с CH,CH H4C. D нс CH2CH3 CH3 "NH, нс Сн HECH...
can you double check these answers?
11. Consider the Grignard reaction below to answer the following question(s). HO muchopnice electronice 3.CH Mg ch нс CH, 2 Hot : A the alcohol product can be classified as a .3 alcanot The nucleophile in this reaction is: 1' alcohol 2' alcohol 3' alcohol 4 alcohol 12. To answer the following question(s), consider the reaction below: OH POCH Pyridine CH CH3 Draw arrows which account for the complete stepwise mechanism for this reaction....
Assign R, S configurations to each indicated chirality center in the molecules below. B. COOH A. OH HOW -H CHANH HNCH HO norepinephrine alamine HOC / OH CH3 не HC HÓ COH tartaric acid CH2 dihadrocarpone The configuration of this carbon atom (A) is · (2 pts.) The configuration of this carbon atom (B) is _ . (2 pts.) The configuration of this carbon atom (C) is . (2 pts.) . The configuration of this carbon atom (D) is __....
star each asymmetric carbon atom in the following examples
& determine whether it has the R or S configuration
PROBLEM 5-6 Star () each asymmetric carbon atom in the following examples, and determine whether it has the (R) or (S) configuration. сн, Н Н H CH, (c) H. (a) (b) Br но с, CH сH CH, CH,CH НС н н CH, Н (d) (e) (D Н Н Cl H Cl Cl СНO (g) (h) ("i) CH CH, (CH,O),CH CH(CH), D...
could someone answer these for me please
1. Use numbers to indicate which compound will react the fastest by the Ss2 med these alcohols with Nal in acetone. With 1 being the fastest and 4 being the slowest (10 ne lastest by the S2 mechanism for нс , H₂C нсон, Br H₂C * now the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CHE conc. HBr CH, HCM Syl condition...
7. Refer to Exhibit 5-3. The configuration of this carbon atom (E) 15 Exhibit 5-4 Consider the structure of streptimidone to answer the following question(s): OH OH нс н stopuklone ĄCH 8. Refer to Exhibit 5-4. Assign Ror Sconfiguration to each chirality center indicated in streptimidone. 9. Refer to Exhibit 5-4. Will streptimidone have a meso stereoisomer? Explain your answer. Exhibit 5-5 Label each pair of stereoisomers below as: a. enantiomers b. diastereomers c. identical Place the letter of the...
For
each of the structures below draw the alcohol that would be
predominatly formed from the hydration (an addition reaction) of
the double bond.
For each of the structures below draw the alcohol that would be predominantly formed from the hydration (an addition reaction) of the double bond. 10. H3C-CH==CH2 + H2O 11. + H2O - H₂CC=CH₂ + H₂O нс CH2 + H₂O CH3 3 + H₂O
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What is the product of this bromination reaction? H2C-CH=CH-CH2-CH2-CH3 + Br2 3. What is the product of this oxidation reaction? OH H3C-CH-CH-CHg 10 Сн, 4. Consider the esterification reaction reaction below: H, SO H3C-CH2-CH2-CH2-C-OH + H2C-CH2-OH What organic compound is the reactant on the left? What organic compound is the reactant on the right? Draw the product of the reaction. What type of organic compound...
Predict the products formed in the following reactions.
Predict the product(s) formed in the following reactions. If there is no reaction, write “No Rxn" as the answer for the major product and leave the minor product box blank. If there is no minor product in the reaction, then leave the minor product box blank. If there are multiple products, make sure the products are in the appropriate box. (24 points, 4 points each) Note: Do not over complicate some questions...
Assign R, S configurations to each indicated che e se A. OH! HO TTCH NH, merupp hale HOC / OH H HO HC COZH acid tarber CH, 1. The configuration of this carbon atom (A) is 2. The configuration of this carbon atom (B) is 3. The configuration of this carbon atom (E) is Consider the structure of streptimidone to answer the following question(s). OH OH strep timidone H3C H 4. Assign R or S configuration to each chirality center...
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