One of the compounds present in lanolin was isolated, purified, and then treated with aqueous sodium hydroxide to yield an unbranched alcohol with 20 carbon atoms and an unbranched carboxylic acid wit...
One of the compounds present in lanolin was isolated, purified,
and then treated with aqueous sodium hydroxide to yield an
unbranched alcohol with 20 carbon atoms and an unbranched
carboxylic acid with 22 carbon atoms. Draw the structure of the
compound:
Homework Answers
Hydrolysis of ester generates carboxylic acid and alcohol.
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One of the compounds present in lanolin was isolated, purified, and then treated with aqueous sodium hydroxide to yield an unbranched alcohol with 20 carbon atoms and an unbranched carboxylic acid wit...
When the cyclopropenyl alcohol (C13H280) below is generated and treated immediately with aqueous perchloric acid (HCIO),...
When the cyclopropenyl alcohol (C13H280) below is generated and treated immediately with aqueous perchloric acid (HCIO), A (C13H27C104) is obtained as stable white crystals. Draw the structure of the CsH27 portion of A. aqueous HCIO C15H27C104 A, m.p. 248-250° dec. not isolated • Draw cations and anions in separate sketchers. • Separate structures with + signs from the drop-down menu.
Questions and Exercises 1. In the course of reflux of the triglyceride in a sodium hydroxide solu...
Organic Chemistry Help!
Questions and Exercises 1. In the course of reflux of the triglyceride in a sodium hydroxide solution you will notice a lot of foaming. Explain. What is left behind in the aqueous layer after filtration of the saponification product? The starting material and the product of the saponification reaction have similar melting points. How do you know you actually isolated a new product rather than just recovered the starting material? Give at least two different methods to...
2. Explain why broad absorbances are expected for compounds containing alcohol and carboxylic acid functional groups....
2. Explain why broad absorbances are expected for compounds containing alcohol and carboxylic acid functional groups. Draw the hydrogen bonding interaction between two ethanol molecules. 3. Draw a compound with a sterically hindered alcohol functional group. What is the most important and distinctive absorbance expected when assessing an IR of this compound? 5. Can IR spectroscopy easily be used to determine the structure of a molecule? Why or why not?
1Ozonolysis of alkenes yields Alcohol carboxylic acid b-ketones if one of the unsaturated carbon atoms is...
1Ozonolysis of alkenes yields Alcohol carboxylic acid b-ketones if one of the unsaturated carbon atoms is disubstituted d- alkane 23-Aldehyde C-0 is more polarized than ketone C-O because a-As in carbocations, more alkyl groups stabilize + character b-Ketone has more alkyl groups, stabilizing the C-O carbon inductively c- due to a andb d- none of the above 24-Aldehydes and unhindered ketones react with HCN to form a-Cyanohydrine b-alcohol c- alkyne d- alkene 25-addition of a Grignard reagent to formaldehyde followed...
Can someone help with the 4 POST LAB questions thanks Carboxylic Acids and Esters acid). like...
Can someone help with the 4 POST LAB questions thanks
Carboxylic Acids and Esters acid). like citric acid. Face crearboxyl the name implies, a Carbexylic Aclds A salad dressing made of The sour taste of fruits such as lemons is due to the presence of acids like citric acid. tcarboxyl a-hydroxy acids such functional group - that is, a carbonyl group attached to a hydroxyl group. AS dicarboxylic acid carboxylic acid of benzene is called benzoic acid (Figure 1). oil...
7. Draw the structure of a wax formed from a 30-carbon straight chain alcohol and each...
7. Draw the structure of a wax formed from a 30-carbon straight chain alcohol and each carboxylic acid a. lauric acid b. myristic acid c. CH(CH3),COOH 8. What hydrolysis products are formed when each wax is treated with aqueous sulfurie acid? a. CH (CH)COO(CH2)2CH. b. CH:(CH2)24COO(CH2CH, c. CH(CH3)COO(CH2).CH; 9. Draw a triacylglycerol that fits each description: a. A triacylglycerol formed from two molecules of lauric acid and one molecule of palmitic acid b. A polyunsaturated triacylglycerol formed from three molecules...
One of the most important uses for Grignard reagents is their addition to carbonyl compounds to...
One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the second step to protonate the alkoxide ion and form the product alcohol. Draw the structure of the product(s) of step 1 when the following compound reacts with...
MyChart-Login Page the crux &Montana Google Drive GRE C Chems 2 WebExpressHome Page-Army Av.... Cengage troy utilities Hydrocarbon A reacts with cold aqueous sulfuric acid to give an alcohol...
MyChart-Login Page the crux &Montana Google Drive GRE C Chems 2 WebExpressHome Page-Army Av.... Cengage troy utilities Hydrocarbon A reacts with cold aqueous sulfuric acid to give an alcohol, B (CAHI00). A also reacts with borane in anhydrous THF followed by hydrogen peroxide in aqueous sodium hydroxide to give an isomeric alcohol C. Draw the structure of A. You do not have to consider stereochemistry . In cases where there is more than one answer, just draw one. Previous Rety...
I need help with the excercises listed on the first page: 18 and 19 18. Complete...
I
need help with the excercises listed on the first page: 18 and
19
18. Complete each of the following reactions. Then determine where the equilibrium is moving it is say which one favors the formation of the reactants and which one favors the formation of the products. If you cannot decide with the structure, compare the pka value of the acid with that of the conjugate acid. 4. CHỊCH NH • Hỏi - CHCH-CC-H.H c. CHOH + H-Br =...
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectivene...
please answer all these questions, thank you.
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...
When the cyclopropenyl alcohol (C13H280) below is generated and treated immediately with aqueous perchloric acid (HCIO), A (C13H27C104) is obtained as stable white crystals. Draw the structure of the CsH27 portion of A. aqueous HCIO C15H27C104 A, m.p. 248-250° dec. not isolated • Draw cations and anions in separate sketchers. • Separate structures with + signs from the drop-down menu.
Organic Chemistry Help!
Questions and Exercises 1. In the course of reflux of the triglyceride in a sodium hydroxide solution you will notice a lot of foaming. Explain. What is left behind in the aqueous layer after filtration of the saponification product? The starting material and the product of the saponification reaction have similar melting points. How do you know you actually isolated a new product rather than just recovered the starting material? Give at least two different methods to...
1Ozonolysis of alkenes yields Alcohol carboxylic acid b-ketones if one of the unsaturated carbon atoms is disubstituted d- alkane 23-Aldehyde C-0 is more polarized than ketone C-O because a-As in carbocations, more alkyl groups stabilize + character b-Ketone has more alkyl groups, stabilizing the C-O carbon inductively c- due to a andb d- none of the above 24-Aldehydes and unhindered ketones react with HCN to form a-Cyanohydrine b-alcohol c- alkyne d- alkene 25-addition of a Grignard reagent to formaldehyde followed...
Can someone help with the 4 POST LAB questions thanks
Carboxylic Acids and Esters acid). like citric acid. Face crearboxyl the name implies, a Carbexylic Aclds A salad dressing made of The sour taste of fruits such as lemons is due to the presence of acids like citric acid. tcarboxyl a-hydroxy acids such functional group - that is, a carbonyl group attached to a hydroxyl group. AS dicarboxylic acid carboxylic acid of benzene is called benzoic acid (Figure 1). oil...
7. Draw the structure of a wax formed from a 30-carbon straight chain alcohol and each carboxylic acid a. lauric acid b. myristic acid c. CH(CH3),COOH 8. What hydrolysis products are formed when each wax is treated with aqueous sulfurie acid? a. CH (CH)COO(CH2)2CH. b. CH:(CH2)24COO(CH2CH, c. CH(CH3)COO(CH2).CH; 9. Draw a triacylglycerol that fits each description: a. A triacylglycerol formed from two molecules of lauric acid and one molecule of palmitic acid b. A polyunsaturated triacylglycerol formed from three molecules...
One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the second step to protonate the alkoxide ion and form the product alcohol. Draw the structure of the product(s) of step 1 when the following compound reacts with...
MyChart-Login Page the crux &Montana Google Drive GRE C Chems 2 WebExpressHome Page-Army Av.... Cengage troy utilities Hydrocarbon A reacts with cold aqueous sulfuric acid to give an alcohol, B (CAHI00). A also reacts with borane in anhydrous THF followed by hydrogen peroxide in aqueous sodium hydroxide to give an isomeric alcohol C. Draw the structure of A. You do not have to consider stereochemistry . In cases where there is more than one answer, just draw one. Previous Rety...
I
need help with the excercises listed on the first page: 18 and
19
18. Complete each of the following reactions. Then determine where the equilibrium is moving it is say which one favors the formation of the reactants and which one favors the formation of the products. If you cannot decide with the structure, compare the pka value of the acid with that of the conjugate acid. 4. CHỊCH NH • Hỏi - CHCH-CC-H.H c. CHOH + H-Br =...
please answer all these questions, thank you.
CHEM 242L Exp. 4 Report/ Synthesis of Oil of Wintergreen Name Score: 20 1) Assess the effectiveness of the experiment and your technique by A) reporting the yield of each step in grams and percent as well as the overall percent yield (What is "overall percent yield?). SHOW ALL CALCULATIONS! B) Give a complete analysis of the identity and purity of your final product and any isolated intermediates 2 What was the purpose...
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