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I need help with all of those questions 1to 10
dr Discover the Viking Experie dr...
I need help on all of these please 1. Draw the energy diagram that correctly depicts...
I need help on all of these please
1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
instructions: Record these transactions in the general journal for Central Advertising Inc. Then post your journal...
instructions: Record these transactions in the general journal for Central Advertising Inc. Then post your journal entries in the t-accounts provided and prepare a trial balance. You may want to refer to Part 1 of this project where you have already analyzed these transactions. 84 General Journal You invested $13,000 in exchange for common stock to start Central Advertising Date Account PR Debt Credit 84 Purchased 6 months of insurance for $1500 cash 87 Purchased $8,000 of office equipment by...
3. a. List the and state if( ) (10 pts ca.) i. Nucleophile (strong/weak), Basicity (strong/weak)...
3. a. List the and state if( ) (10 pts ca.) i. Nucleophile (strong/weak), Basicity (strong/weak) ii. Substrate (1°/2°/3°) iii. Leaving group (good/poor) iv. Solvent (protic/aprotic) b. Label the mechanism for the reaction (S1/S2/E1/E2) c. Draw the mechanism for the reactions and predict the major product(s). Use proper stereochemistry where necessary d. State which is the rate determining step (RDS) e. Give a rate law for each reaction. Ex: Rate=K[ A B NaSCH CH2CN OH HI MeOH
+ Fit to page Page view 1. (10 pts) For the following reactions: a. Label the...
+ Fit to page Page view 1. (10 pts) For the following reactions: a. Label the Nucleophile (Nu) and whether it is strong or weak b. Label the Electrophile (E) and whether it is primary, secondary, or tertiary and circle the leaving group c. Label the Solvent and whether it is polar protic or polar aprotic d. Categorize each as preferring SN1, Preferring SN2, or could do either e Draw the product of the reaction, based upon your categorization, remember...
HWS 5: Due 10/30/2019 15 points total SN1, SN2, Elimination pt 1 1. (10 pts) For...
HWS 5: Due 10/30/2019 15 points total SN1, SN2, Elimination pt 1 1. (10 pts) For the following reactions: a. Label the Nucleophile (Nu) and whether it is strong or weak b. Label the Electrophile (E) and whether it is primary, secondary, or tertiary and circle the leaving group C. Label the Solvent and whether it is polar protic or polar aprotic d. Categorize each as preferring SN1, Preferring SN2, or could do either e. Draw the product of the...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
I need help with #2 please explain step by step. POST LAB QUESTIONS 1. Predict all possible bromination products of...
I need help with #2 please explain step by step.
POST LAB QUESTIONS 1. Predict all possible bromination products of the following substrate using the above reaction conditions. Show stereochemistry (i.e. dashed and wedged bonds, and label chiral centers (R or S), if necessary. Dogou or dilbi o bando sobre in the manica Br2 YCHE CH3 2. A researcher performs the above reaction starting with 0.150 g of the alkene substrate, 0.375 g of pyridinium tribromide, and 2.00 mL of...
Organic chemistry mechanisms i need help with systheses questions 6,7,8,9 2-hydroxybenzoic (3 pts) 5. Provide an...
Organic chemistry mechanisms
i need help with systheses questions 6,7,8,9
2-hydroxybenzoic (3 pts) 5. Provide an appropriate structure for: 3,3-dimethylcyclobutanecarbonitrile. (4 pts each, unless otherwise noted, 12 pts total) 6-8. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does...
I need help on all of these please
1. Draw the energy diagram that correctly depicts the following reaction (AG<0) and the transition state for the rate determining step. Label substrate (S), product (P), and intermediate (1) if applicable. OTS + NaBr TsONa polar aprotic solvent transition state free energy reaction progress 2. Complete the following reaction schemes. CH3OH 0°C alkyl halide nucleophile ТА polar aprotic solvent 3. Compound A and B are constitutional isomers with molecular formula C5H11Br. When...
instructions: Record these transactions in the general journal for Central Advertising Inc. Then post your journal entries in the t-accounts provided and prepare a trial balance. You may want to refer to Part 1 of this project where you have already analyzed these transactions. 84 General Journal You invested $13,000 in exchange for common stock to start Central Advertising Date Account PR Debt Credit 84 Purchased 6 months of insurance for $1500 cash 87 Purchased $8,000 of office equipment by...
3. a. List the and state if( ) (10 pts ca.) i. Nucleophile (strong/weak), Basicity (strong/weak) ii. Substrate (1°/2°/3°) iii. Leaving group (good/poor) iv. Solvent (protic/aprotic) b. Label the mechanism for the reaction (S1/S2/E1/E2) c. Draw the mechanism for the reactions and predict the major product(s). Use proper stereochemistry where necessary d. State which is the rate determining step (RDS) e. Give a rate law for each reaction. Ex: Rate=K[ A B NaSCH CH2CN OH HI MeOH
+ Fit to page Page view 1. (10 pts) For the following reactions: a. Label the Nucleophile (Nu) and whether it is strong or weak b. Label the Electrophile (E) and whether it is primary, secondary, or tertiary and circle the leaving group c. Label the Solvent and whether it is polar protic or polar aprotic d. Categorize each as preferring SN1, Preferring SN2, or could do either e Draw the product of the reaction, based upon your categorization, remember...
HWS 5: Due 10/30/2019 15 points total SN1, SN2, Elimination pt 1 1. (10 pts) For the following reactions: a. Label the Nucleophile (Nu) and whether it is strong or weak b. Label the Electrophile (E) and whether it is primary, secondary, or tertiary and circle the leaving group C. Label the Solvent and whether it is polar protic or polar aprotic d. Categorize each as preferring SN1, Preferring SN2, or could do either e. Draw the product of the...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
I need help with #2 please explain step by step.
POST LAB QUESTIONS 1. Predict all possible bromination products of the following substrate using the above reaction conditions. Show stereochemistry (i.e. dashed and wedged bonds, and label chiral centers (R or S), if necessary. Dogou or dilbi o bando sobre in the manica Br2 YCHE CH3 2. A researcher performs the above reaction starting with 0.150 g of the alkene substrate, 0.375 g of pyridinium tribromide, and 2.00 mL of...
Organic chemistry mechanisms
i need help with systheses questions 6,7,8,9
2-hydroxybenzoic (3 pts) 5. Provide an appropriate structure for: 3,3-dimethylcyclobutanecarbonitrile. (4 pts each, unless otherwise noted, 12 pts total) 6-8. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does...
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