Compound A, C11H12O, which gave a negative Tollens test, was treated with LiAlH4, followed by dilute...
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Compound A, C11H12O, which gave a negative Tollens test, was treated with LiAlH4, followed by dilute...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyri...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
When the epoxide 2‑vinyloxirane reacts with lithium dibutylcuprate, followed by protonolysis, compound A is the major product formed. Oxidation of A with PCC yields B, a compound that gives a positive Tollens test and has an intense UV absorption around 2
When the epoxide 2‑vinyloxirane reacts with lithium dibutylcuprate, followed by protonolysis, compound A is the major product formed. Oxidation of A with PCC yields B, a compound that gives a positive Tollens test and has an intense UV absorption around 215 nm. Treatment of B with Ag2O,Ag2O, followed by catalytic hydrogenation, gives octanoic acid. Identify A and B.
Chemistry help please 3 easy questions 3. Which are the correct configurations of the two chirality...
Chemistry help please 3 easy
questions
3. Which are the correct configurations of the two chirality centers (stereocenters) in the following Fischer projection? CHO H HO ОН H CH2OH A. 2R, 3R B. 2R, 3S C. 2S, 3R D. 2S, 3S 4. When a sugar was treated with warm nitric acid it gave an optically active compound. Wohl degradation of the same sugar gave L-glyceraldehyde. The structure of the sugar is CHO -ОН H HO H CHO HO -H HO...
Three bottles A, B, and C have been found, each of which contains aliquid and...
Three bottles A, B, and C have been found, each of which contains a
liquid and is labeled \"amine C8H11N.\" As an expert in amine
chemistry, you have been hired as a consultant and asked to
identify each compound. Compounds A and B give off a gas when they
react with NaNO2 and HCl at 0 ℃; C does not. However, when the
aqueous reaction mixture from the diazotization of C is warmed, a
gas is evolved. Compound A is...
identify which compound is more acidic and explain your choice. or each of the following compounds,...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
13. What can you say about an unknown compound that gave a pouldve test with 2...
13. What can you say about an unknown compound that gave a pouldve test with 2 hydrazine and a positive test with the Jones Reseat? now compound that gave a pouldve test with 2,4-dinitrophenyl 14 What can you say about sa unknown compound when dissolved in distilled water and tested with peper, pave an estimated pH of about 81. 15. What can you say about an unknown compound that turned a wet plece al blue litmus red? 16. What can...
6 In Part C, which of the anta heartburn? Use the information you o which of the antacids you tested would b...
6 In Part C, which of the anta heartburn? Use the information you o which of the antacids you tested would be the most effective at neutralizing stomach acid to w a offerences in the effectiveness of the antacids you tested e the information you obtained from the antacid package labels to offer an explanation for the some antacids produce bubbles when they react with acids. The bubbles are carbon dioxide (CO) released by decomposition of carbonic acid (H.CO) produced...
Please help with pre-lab questions. Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation...
Please help with pre-lab questions.
Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation of +3.25. Determine the optical purity (%ee) and percent composition of this sample (see Mohrig section 17.4). The specific rotation of pure (+)-2-butanol is +13.0°. 2. The equation for the formation of the diastereomeric salts is shown in the background information (performed in Part A of the procedure). Write this chemical equation in your notebook, then ALSO write a balanced equation for the formation...
Can you help me determine if I am correct and help me find the ither answers...
Can
you help me determine if I am correct and help me find the ither
answers to this functional group lab worksheet?
18 w paper 1 we by addin trecome char Discussion of Properties and Test Ora general undergo dition reactions, whereas by substitution reactions. These two types of d e beds and womate compounds we characterized described in equation form as follows: action Addition Reaction Substitution Reaction (Note: numbers in boxes to the left refer to w in the...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Chemistry help please 3 easy
questions
3. Which are the correct configurations of the two chirality centers (stereocenters) in the following Fischer projection? CHO H HO ОН H CH2OH A. 2R, 3R B. 2R, 3S C. 2S, 3R D. 2S, 3S 4. When a sugar was treated with warm nitric acid it gave an optically active compound. Wohl degradation of the same sugar gave L-glyceraldehyde. The structure of the sugar is CHO -ОН H HO H CHO HO -H HO...
Three bottles A, B, and C have been found, each of which contains a
liquid and is labeled \"amine C8H11N.\" As an expert in amine
chemistry, you have been hired as a consultant and asked to
identify each compound. Compounds A and B give off a gas when they
react with NaNO2 and HCl at 0 ℃; C does not. However, when the
aqueous reaction mixture from the diazotization of C is warmed, a
gas is evolved. Compound A is...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
13. What can you say about an unknown compound that gave a pouldve test with 2 hydrazine and a positive test with the Jones Reseat? now compound that gave a pouldve test with 2,4-dinitrophenyl 14 What can you say about sa unknown compound when dissolved in distilled water and tested with peper, pave an estimated pH of about 81. 15. What can you say about an unknown compound that turned a wet plece al blue litmus red? 16. What can...
6 In Part C, which of the anta heartburn? Use the information you o which of the antacids you tested would be the most effective at neutralizing stomach acid to w a offerences in the effectiveness of the antacids you tested e the information you obtained from the antacid package labels to offer an explanation for the some antacids produce bubbles when they react with acids. The bubbles are carbon dioxide (CO) released by decomposition of carbonic acid (H.CO) produced...
Please help with pre-lab questions.
Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation of +3.25. Determine the optical purity (%ee) and percent composition of this sample (see Mohrig section 17.4). The specific rotation of pure (+)-2-butanol is +13.0°. 2. The equation for the formation of the diastereomeric salts is shown in the background information (performed in Part A of the procedure). Write this chemical equation in your notebook, then ALSO write a balanced equation for the formation...
Can
you help me determine if I am correct and help me find the ither
answers to this functional group lab worksheet?
18 w paper 1 we by addin trecome char Discussion of Properties and Test Ora general undergo dition reactions, whereas by substitution reactions. These two types of d e beds and womate compounds we characterized described in equation form as follows: action Addition Reaction Substitution Reaction (Note: numbers in boxes to the left refer to w in the...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
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