For number 2, would someone be able to explain the mechanism to me in words rather than structures?
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For number 2, would someone be able to explain the mechanism to
me in words rather...
Question 1 What is the mechanism of the synthesis of methyl salicylate? esterification Sn1 SnAcyl AnE Question 2 Which compound is responsible for the burnt-fat odor in the test for gly...
Question 1 What is the mechanism of the synthesis of methyl salicylate? esterification Sn1 SnAcyl AnE Question 2 Which compound is responsible for the burnt-fat odor in the test for glycerol? glycerol acrolein acetic acicd o fatty acid Question 3 Which of the following reagents is NOT used for the synthesis of methyl salicylate? o acetic acid methanol salicylic acid sulfuric acid Question 4 Which of the following chemically define a soap? salt of a thoester salt of a carboxylic...
Would someone help me to solve these questions? Thanks in advanced Questions 1. Draw the mechanism...
Would someone help me to solve these questions? Thanks
in advanced
Questions 1. Draw the mechanism of the formation of the diazonium salt from sulfanilic acid. 2. Draw the mechanism of the reaction of N,N-dimethylaniline and the diazonium salt of sulfanilic acid to form the azo dye. 3. Why does the dimethylaniline couple with the diazonium salt at the para position of the ring? 4. What would be the result if copper (I) chloride were added to the diazonium salt...
Can someone tell me if a theoretical yield needs to be calculated for this experiment? And...
Can someone tell me if a theoretical yield needs to be
calculated for this experiment? And if so, how do you calculate it?
please show all work. thank you. btw the aniline weighs
6.69g.
Synthesis of Acetanilide Acetanilide is synthesized from aniline by a reaction known as acylation. Acylation is the addition of an acyl group to a compound. In this experiment, aniline (1 amine) is reacted with acetic anhydride (acylating agent) to form acetanilide (an amide). H-C-CH3 + CH...
if someone could show me how to do all of these, that would be great Acids...
if
someone could show me how to do all of these, that would be
great
Acids and Bases Name Directions: Answer/Calclulate the following. Use a separate sheet if needed. Give the Arrhenius and Bronsted/Lowry definitions for acids and bases. How are they similar and different? In the Bronsted/Lowry definition, acids and bases always occur If an equation is "looked at in reverse", then the acid becomes the -. These are known and the base becomes Identify the acid, base, conjugate...
just need (e) to (h) 5. Molecules with an-OH group directly bonded to a C-C sp...
just need (e) to (h)
5. Molecules with an-OH group directly bonded to a C-C sp hybridized carbon are called "enol"'s. The types of chemical reactions which enols undergo are substantially different from those of normal alcohols. By considering the Brensted-Lowry and Lewis acid/base reactivity of an enol, you can predict a few of these differences. (a) Ethenol, the simplest "enol", can react as a BL. base in three different places, by gaining a proton at either of the two...
2. Draw the structure of the byproduct that would be formed if the reaction mixture were...
2. Draw the structure of the byproduct that would be formed if the reaction mixture were not kept in an ice bath during the azo coupling reaction. [2 pts) Methyl orange can be synthesized using an azo coupling reaction, which is an example of an electrophilic aromatic substitution (EAS). In an azo coupling, the electrophile is an aryldiazonium salt, and the nucleophile is another electron-rich aromatic compound (typically an aniline or phenol). In this experiment, sulfanilic acid will be converted...
20.14 ULUS because they result in the transfer of an wety np. from one heterontom to...
20.14
ULUS because they result in the transfer of an wety np. from one heterontom to another is prepared by the acetylation of morphine, an analyesic compound Isolated from the opium poppy. Both OH groups of morphine are readily acetylated with ceris whydride to form the diester present in heroin. HO OT o HF HOW Problem 20.14 morphine heroin minyarides react like acid chlorides with the nucleophiles described in Chapter 17. draw the products formed when each of the following...
Would somebody be able to help me with these 2. (6 points) The rearrangement of cyclopropane...
Would somebody be able to help me with these
2. (6 points) The rearrangement of cyclopropane (C3Hs) to propene (C34) is a first-order reaction, with a rate constant (k) 6.7x 104 s1 at 773 K 0.25 mol of C3H6 is placed in a 5 L container. (i) What is the concentration (M) of C3Hs after 30 minutes? (ii) How long does it take for the C3H6 concentration to drop to 0.010 M? (iii ) How long does it take for...
Please show detailed mechanism or explain in words. DQ25.11 Homework Draw the starting material: . SOCI,...
Please show detailed mechanism or explain in words.
DQ25.11 Homework Draw the starting material: . SOCI, DMF 2. (CH,CH),CuLi, THF Ph 3. H,O Hint: Note that organocuprates only add once to acyl chlorides. DQ25.12 Homework Draw the product of the following reactions: 0 O HN CH CI NaBH (1 equiv.) EtOH Hint: Think about the reactivity of the carboxylic acid derivatives. DQ25.13 Homework Draw the product of the following reaction. CH,NO cc, tBuOK, DMSO CCI Hint: The first step in...
Can someone please predict the major products and PLEASE put the mechanism so I know how...
Can someone please predict the major products and PLEASE put the
mechanism so I know how the products were achieved.
Problem #1 Predict the major product(s) from the following reactions: a) 1. O3 CH3 2. DMS CH3 b) 1. CH3CO3H ? 2. H30* CH3 cat. OsO4 - CH3 t-BuOOH d) CH3 KMnO4 cold CH3 e) CHs .CHa На Нас ? Pt CHs f) CH3 1. BH3-THF Нас ? CH3 2. H2O, NaOH g) Br2 CH3OH CHa Extra Credit An unknown...
Question 1 What is the mechanism of the synthesis of methyl salicylate? esterification Sn1 SnAcyl AnE Question 2 Which compound is responsible for the burnt-fat odor in the test for glycerol? glycerol acrolein acetic acicd o fatty acid Question 3 Which of the following reagents is NOT used for the synthesis of methyl salicylate? o acetic acid methanol salicylic acid sulfuric acid Question 4 Which of the following chemically define a soap? salt of a thoester salt of a carboxylic...
Would someone help me to solve these questions? Thanks
in advanced
Questions 1. Draw the mechanism of the formation of the diazonium salt from sulfanilic acid. 2. Draw the mechanism of the reaction of N,N-dimethylaniline and the diazonium salt of sulfanilic acid to form the azo dye. 3. Why does the dimethylaniline couple with the diazonium salt at the para position of the ring? 4. What would be the result if copper (I) chloride were added to the diazonium salt...
Can someone tell me if a theoretical yield needs to be
calculated for this experiment? And if so, how do you calculate it?
please show all work. thank you. btw the aniline weighs
6.69g.
Synthesis of Acetanilide Acetanilide is synthesized from aniline by a reaction known as acylation. Acylation is the addition of an acyl group to a compound. In this experiment, aniline (1 amine) is reacted with acetic anhydride (acylating agent) to form acetanilide (an amide). H-C-CH3 + CH...
if
someone could show me how to do all of these, that would be
great
Acids and Bases Name Directions: Answer/Calclulate the following. Use a separate sheet if needed. Give the Arrhenius and Bronsted/Lowry definitions for acids and bases. How are they similar and different? In the Bronsted/Lowry definition, acids and bases always occur If an equation is "looked at in reverse", then the acid becomes the -. These are known and the base becomes Identify the acid, base, conjugate...
just need (e) to (h)
5. Molecules with an-OH group directly bonded to a C-C sp hybridized carbon are called "enol"'s. The types of chemical reactions which enols undergo are substantially different from those of normal alcohols. By considering the Brensted-Lowry and Lewis acid/base reactivity of an enol, you can predict a few of these differences. (a) Ethenol, the simplest "enol", can react as a BL. base in three different places, by gaining a proton at either of the two...
2. Draw the structure of the byproduct that would be formed if the reaction mixture were not kept in an ice bath during the azo coupling reaction. [2 pts) Methyl orange can be synthesized using an azo coupling reaction, which is an example of an electrophilic aromatic substitution (EAS). In an azo coupling, the electrophile is an aryldiazonium salt, and the nucleophile is another electron-rich aromatic compound (typically an aniline or phenol). In this experiment, sulfanilic acid will be converted...
20.14
ULUS because they result in the transfer of an wety np. from one heterontom to another is prepared by the acetylation of morphine, an analyesic compound Isolated from the opium poppy. Both OH groups of morphine are readily acetylated with ceris whydride to form the diester present in heroin. HO OT o HF HOW Problem 20.14 morphine heroin minyarides react like acid chlorides with the nucleophiles described in Chapter 17. draw the products formed when each of the following...
Would somebody be able to help me with these
2. (6 points) The rearrangement of cyclopropane (C3Hs) to propene (C34) is a first-order reaction, with a rate constant (k) 6.7x 104 s1 at 773 K 0.25 mol of C3H6 is placed in a 5 L container. (i) What is the concentration (M) of C3Hs after 30 minutes? (ii) How long does it take for the C3H6 concentration to drop to 0.010 M? (iii ) How long does it take for...
Please show detailed mechanism or explain in words.
DQ25.11 Homework Draw the starting material: . SOCI, DMF 2. (CH,CH),CuLi, THF Ph 3. H,O Hint: Note that organocuprates only add once to acyl chlorides. DQ25.12 Homework Draw the product of the following reactions: 0 O HN CH CI NaBH (1 equiv.) EtOH Hint: Think about the reactivity of the carboxylic acid derivatives. DQ25.13 Homework Draw the product of the following reaction. CH,NO cc, tBuOK, DMSO CCI Hint: The first step in...
Can someone please predict the major products and PLEASE put the
mechanism so I know how the products were achieved.
Problem #1 Predict the major product(s) from the following reactions: a) 1. O3 CH3 2. DMS CH3 b) 1. CH3CO3H ? 2. H30* CH3 cat. OsO4 - CH3 t-BuOOH d) CH3 KMnO4 cold CH3 e) CHs .CHa На Нас ? Pt CHs f) CH3 1. BH3-THF Нас ? CH3 2. H2O, NaOH g) Br2 CH3OH CHa Extra Credit An unknown...
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