Could someone help with these two questions?
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Could someone help with these two questions?
3. (3p) What reagent is necessary in the hydrolysis...
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: xo 2....
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: xo 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity. 4. (3p) Write the product for the following reaction: NaOH CHO 5. (3p) Propose a synthesis for the following compound by using a Witting reaction:
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: 2. (3p)...
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: OH 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity.
Questions 12-20 are true and false! (12) Hydrolysis of nitriles is a method to synthesize carboxylic...
Questions 12-20 are true and false!
(12) Hydrolysis of nitriles is a method to synthesize carboxylic acid. (13) The order of reactivity of carboxylic acid derivatives is as follow: Acyl chloride > Acid anhydride > Ester > Amide. (14) SOCI2, PC13 and PCls are three types of special reagents to convert carboxylic acid to acyl chloride (15) Acyl chlorides are the most reactive common acyl derivatives, and can be used to synthesize anhydride, ester, and amide. (16) Acyl chloride is...
If someone could help me out with these two that would be great! 18. Arrange the...
If
someone could help me out with these two that would be great!
18. Arrange the following compounds in order of reactivity (with highest being 1) and explain your order. CHC-WH, MC-G CHC-CH, 19. Explain why the acid chloride instead of the carboxylic acid is used to react with an amine to make an amide.
If someone could help me out with these questions that would be much appreciated! of the...
If
someone could help me out with these questions that would be much
appreciated!
of the following Fisher esterification 20. Draw the mechanism reaction: a hou die media of the surning toket certain Obmo H.SO + CH OH 21. Compound A can be converted to the carboxylic acid B by Grignard carboxylation or nitrile hydrolysis which method would you use, and why. CH.
can someone help me solve these Question 3 What reagent can be used to prepare the...
can someone help me solve these
Question 3 What reagent can be used to prepare the following compound in the highest yield? CH, 1. Reagent HC НАС 2. CHE! ОЕТОН OLDA NaOET он20 o B a * Pawi Question 4 What is the major product of the following reaction? excess Kobu Product 0 OBu 0 OtBu 0 0 of a Question 6 What would be the major product of the following reaction sequence? taba = - = OOO = =
could I get some help please, thankyou very much in advance. [ 0 。 ་། 2....
could I get some help please, thankyou very much in
advance.
[ 0 。 ་། 2. One of the key transformations of a carboxylic acid is reduction to an alcohol Provide the missing product for the first scheme and missing reagent(s) for the second schone shown below. 3. Carboxylic acids are particularly useful when transformed into carboxylic acid derivatives where the OH group is replaced with some other atom or group Acid chlondes are a particularly versatile in transformations Provide...
I need help with these questions please! 3. What are the hydrolysis products in the reaction...
I need help with these questions please!
3. What are the hydrolysis products in the reaction below? Coba 4. Determine if the IR spectrums below belong to benzoic acid or methyl benozate. What are the important types of bonds on each IR spectrum? And what are the bonds frequencies on both IR spectrums? ---------- LAULUDED BELIEU ------------ The IR spectrum for benzaldehyde is below. Identify the bonds that absorb at the following wavenumbers. 3086 cm-1 2860 and 2736 cm-1 1703...
could someone please answer these 3 questions? 2. What product would you expect from the following...
could someone please answer these 3
questions?
2. What product would you expect from the following reaction? ÇOCH B ÇOCH A oi CO2CH3 B ÇOCH E. CO2CH3 4. What will be the best way to synthesize the following compound starting from benzene? D CO2CH3 8 E A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI; 2) Zn, HCI; 3) Cl2, FeCls;...
I need help with this spider diagram complete the following diagram that illustrates the reactivity of...
I need help with this spider diagram
complete the following diagram that illustrates the reactivity of the carboxylic acid derivatives de se une structures provided (A-H) and the reaction conditions shown below (1-10). You may use the reas shown more then once if necessary. Structures: Reaction Conditions: SNH2 (204) 1) H202 ) SOCI23) HCI, H20, heat 5) H2SO4. PrOH 7) IPOH 8) NaOH, H2O HNL (209) 18 Non Complete the following...
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: xo 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity. 4. (3p) Write the product for the following reaction: NaOH CHO 5. (3p) Propose a synthesis for the following compound by using a Witting reaction:
1. (3p) Draw the mechanism and the expected reaction product for the following reaction: 2. (3p) Draw the mechanism and the expected Nucleophilic Substitution Reaction Product for the following reaction: OH 3. (3p) What reagent is necessary in the hydrolysis of carboxylic acid derivatives? Rank these derivatives in order of their reactivity.
Questions 12-20 are true and false!
(12) Hydrolysis of nitriles is a method to synthesize carboxylic acid. (13) The order of reactivity of carboxylic acid derivatives is as follow: Acyl chloride > Acid anhydride > Ester > Amide. (14) SOCI2, PC13 and PCls are three types of special reagents to convert carboxylic acid to acyl chloride (15) Acyl chlorides are the most reactive common acyl derivatives, and can be used to synthesize anhydride, ester, and amide. (16) Acyl chloride is...
If
someone could help me out with these two that would be great!
18. Arrange the following compounds in order of reactivity (with highest being 1) and explain your order. CHC-WH, MC-G CHC-CH, 19. Explain why the acid chloride instead of the carboxylic acid is used to react with an amine to make an amide.
If
someone could help me out with these questions that would be much
appreciated!
of the following Fisher esterification 20. Draw the mechanism reaction: a hou die media of the surning toket certain Obmo H.SO + CH OH 21. Compound A can be converted to the carboxylic acid B by Grignard carboxylation or nitrile hydrolysis which method would you use, and why. CH.
can someone help me solve these
Question 3 What reagent can be used to prepare the following compound in the highest yield? CH, 1. Reagent HC НАС 2. CHE! ОЕТОН OLDA NaOET он20 o B a * Pawi Question 4 What is the major product of the following reaction? excess Kobu Product 0 OBu 0 OtBu 0 0 of a Question 6 What would be the major product of the following reaction sequence? taba = - = OOO = =
could I get some help please, thankyou very much in
advance.
[ 0 。 ་། 2. One of the key transformations of a carboxylic acid is reduction to an alcohol Provide the missing product for the first scheme and missing reagent(s) for the second schone shown below. 3. Carboxylic acids are particularly useful when transformed into carboxylic acid derivatives where the OH group is replaced with some other atom or group Acid chlondes are a particularly versatile in transformations Provide...
I need help with these questions please!
3. What are the hydrolysis products in the reaction below? Coba 4. Determine if the IR spectrums below belong to benzoic acid or methyl benozate. What are the important types of bonds on each IR spectrum? And what are the bonds frequencies on both IR spectrums? ---------- LAULUDED BELIEU ------------ The IR spectrum for benzaldehyde is below. Identify the bonds that absorb at the following wavenumbers. 3086 cm-1 2860 and 2736 cm-1 1703...
could someone please answer these 3
questions?
2. What product would you expect from the following reaction? ÇOCH B ÇOCH A oi CO2CH3 B ÇOCH E. CO2CH3 4. What will be the best way to synthesize the following compound starting from benzene? D CO2CH3 8 E A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI; 2) Zn, HCI; 3) Cl2, FeCls;...
I need help with this spider diagram
complete the following diagram that illustrates the reactivity of the carboxylic acid derivatives de se une structures provided (A-H) and the reaction conditions shown below (1-10). You may use the reas shown more then once if necessary. Structures: Reaction Conditions: SNH2 (204) 1) H202 ) SOCI23) HCI, H20, heat 5) H2SO4. PrOH 7) IPOH 8) NaOH, H2O HNL (209) 18 Non Complete the following...
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