1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid,...
1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid, palmitoleic acid, and an oleic acid.
a. Draw the structure of the triglyceride molecule described above by using line-angle formulas for the hydrocarbon tails.
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1. Imagine a triglyceride molecule is made from the following
three fatty acids: a myristic acid,...
1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid,...
1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid, a palmitoleic acid, and an oleic acid. . Draw the structure of the triglyceride molecule described above by using line-angle formulas for the hydrocarbon tails. b. Write the saponification reaction of this triglyceride molecule in KOH solution to produce potassium soap. Use condensed structural formulas for the hydrocarbon tails. c. Write the condensed structural formula for two insoluble ionic compounds produced when this potassium...
1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid,...
1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid, a palmitoleic acid, and an oleic acid. b. Write the saponification reaction of this triglyceride molecule in KOH solution to produce potassium soap. Use condensed structural formulas for the hydrocarbon tails.
Draw a triacylglycerol (triglyceride) made from glycerol, myristic acid (CH, (CH),COOH , palmitic acid (CH,(CH),COOH), and...
Draw a triacylglycerol (triglyceride) made from glycerol, myristic acid (CH, (CH),COOH , palmitic acid (CH,(CH),COOH), and oleic acid (CH,(CH),CH=CH(CH,),COOH (cis)] . Place palmitic acid at the middle position. Cis/trans isometry is graded; it may help to draw hydrogen atoms associated with the carbon atoms of the double bond. Select Draw Draw Rings More Erase Predict whether this triacylglycerol is a liquid or a solid at room temperature (25 °C). liquid O solid
Draw a triacylglycerol (triglyceride) made from glycerol, myristic acid (CH,(CH),COOH) , palmitic acid [CH,(CH) 14COOH) ,...
Draw a triacylglycerol (triglyceride) made from glycerol, myristic acid (CH,(CH),COOH) , palmitic acid [CH,(CH) 14COOH) , and oleic acid (CH,(CH),CH=CH(CH),COOH(cis)] . Place palmitic acid at the middle position. Cis/trans isometry is graded; it may help to draw hydrogen atoms associated with the carbon atoms of the double bond. Select Draw Rings More Erase Q2Q Predict whether this triacylglycerol is a liquid or a solid at room temperature (25 °C). O solid liquid
4. A list of fatty acids is given below. The number of carbons each contains, as...
4. A list of fatty acids is given below. The number of carbons each contains, as well as the number of double bonds, are listed right after the name. Rank the fatty acids 1-5 from highest melting point to lowest melting point. 1 - highest melting point, 5 - lowest melting point. Palmitic acid (16 carbons, 0 double bonds) Oleic acid (18 carbons, 1 double bond) Linolenic acid (18 carbons, 3 double bonds) Lauric acid (12 carbons, 0 double bonds)...
Please answer all components. Postlab 1) Coconut oil ls omprised of a misture of fatty acids in the form of triglycerides. The most abundant fatty acids in coconut oil are as follows: Lauric acid...
Please answer all components.
Postlab 1) Coconut oil ls omprised of a misture of fatty acids in the form of triglycerides. The most abundant fatty acids in coconut oil are as follows: Lauric acid (48%) oleic acid (6.5%) Myrisitic acid (16%) Palmitic acid (9.5%) Draw the structure of each of these fatty acids: Considering the structures above, explain the relatively high melting point of coconut oll 2) Some oils that are improperly stored (exposed to oxygen) over long periods of...
<F15> Is it possible to predict by calculation the iodine number of this triglyceride? Explain. 5....
<F15> Is it possible to predict by calculation the iodine number of this triglyceride? Explain. 5. Using the triglyceride of question 4, which is an oil, write a reaction showing the conversion of this oil to a solid shortening. <F16> What is the name of this type of reaction? tie <F17> What are the reaction conditions and catalysts needed for this type of reactions? <F18> Rank the following fatty acids: myristic acid, oleic acid, and linolenic acid by increasing Iodine...
I am having trouble is this correct? CH 3a) Provide the definition for a fatty acid...
I am having trouble is this correct?
CH 3a) Provide the definition for a fatty acid long straight Chain hydrocarbon that has an even number of covers and carboxylic acid at the end, 1) 3b) Draw the structure of the molecule formed when the weak acid shown is ionized in water acid Base Congo 10 Hydronin non но CH3-(CH2)io-COOH + H2O (1) CH3-(CH2) 10-Coo + H30" th (6 pts) 4) A triglyceride is an ester made of glycerol and carboxylic...
3) Triglycerides are constructed with one molecule of glycerol forming three ester linkages with (three) long...
3) Triglycerides are constructed with one molecule of glycerol forming three ester linkages with (three) long chain fatty acids. Draw the structure of the triglyceride formed with Arachidonic acid, Linoleic acid, and a-Linolenic acid.
C. Bromine Test for Unsaturation 2. Saturated/Unsaturated 1. Color fades rapidly/persists Fatty acids Stearic acid Oleic...
C. Bromine Test for Unsaturation 2. Saturated/Unsaturated 1. Color fades rapidly/persists Fatty acids Stearic acid Oleic acid Triacylglycerols Safflower oil Olive oil Questions and Problems Q3 a. Draw the condensed structural formulas of stearic acid and oleic acid. Stearic acid Oleic acid b. From the results of Part C, which is more unsaturated: oleic acid or stearic a Explain your reason. From the results of Part C, were safflower oil and olive oil saturated or un rated? Explain your reason.
1. Imagine a triglyceride molecule is made from the following three fatty acids: a myristic acid, a palmitoleic acid, and an oleic acid. . Draw the structure of the triglyceride molecule described above by using line-angle formulas for the hydrocarbon tails. b. Write the saponification reaction of this triglyceride molecule in KOH solution to produce potassium soap. Use condensed structural formulas for the hydrocarbon tails. c. Write the condensed structural formula for two insoluble ionic compounds produced when this potassium...
Draw a triacylglycerol (triglyceride) made from glycerol, myristic acid (CH, (CH),COOH , palmitic acid (CH,(CH),COOH), and oleic acid (CH,(CH),CH=CH(CH,),COOH (cis)] . Place palmitic acid at the middle position. Cis/trans isometry is graded; it may help to draw hydrogen atoms associated with the carbon atoms of the double bond. Select Draw Draw Rings More Erase Predict whether this triacylglycerol is a liquid or a solid at room temperature (25 °C). liquid O solid
Draw a triacylglycerol (triglyceride) made from glycerol, myristic acid (CH,(CH),COOH) , palmitic acid [CH,(CH) 14COOH) , and oleic acid (CH,(CH),CH=CH(CH),COOH(cis)] . Place palmitic acid at the middle position. Cis/trans isometry is graded; it may help to draw hydrogen atoms associated with the carbon atoms of the double bond. Select Draw Rings More Erase Q2Q Predict whether this triacylglycerol is a liquid or a solid at room temperature (25 °C). O solid liquid
4. A list of fatty acids is given below. The number of carbons each contains, as well as the number of double bonds, are listed right after the name. Rank the fatty acids 1-5 from highest melting point to lowest melting point. 1 - highest melting point, 5 - lowest melting point. Palmitic acid (16 carbons, 0 double bonds) Oleic acid (18 carbons, 1 double bond) Linolenic acid (18 carbons, 3 double bonds) Lauric acid (12 carbons, 0 double bonds)...
Please answer all components.
Postlab 1) Coconut oil ls omprised of a misture of fatty acids in the form of triglycerides. The most abundant fatty acids in coconut oil are as follows: Lauric acid (48%) oleic acid (6.5%) Myrisitic acid (16%) Palmitic acid (9.5%) Draw the structure of each of these fatty acids: Considering the structures above, explain the relatively high melting point of coconut oll 2) Some oils that are improperly stored (exposed to oxygen) over long periods of...
<F15> Is it possible to predict by calculation the iodine number of this triglyceride? Explain. 5. Using the triglyceride of question 4, which is an oil, write a reaction showing the conversion of this oil to a solid shortening. <F16> What is the name of this type of reaction? tie <F17> What are the reaction conditions and catalysts needed for this type of reactions? <F18> Rank the following fatty acids: myristic acid, oleic acid, and linolenic acid by increasing Iodine...
I am having trouble is this correct?
CH 3a) Provide the definition for a fatty acid long straight Chain hydrocarbon that has an even number of covers and carboxylic acid at the end, 1) 3b) Draw the structure of the molecule formed when the weak acid shown is ionized in water acid Base Congo 10 Hydronin non но CH3-(CH2)io-COOH + H2O (1) CH3-(CH2) 10-Coo + H30" th (6 pts) 4) A triglyceride is an ester made of glycerol and carboxylic...
3) Triglycerides are constructed with one molecule of glycerol forming three ester linkages with (three) long chain fatty acids. Draw the structure of the triglyceride formed with Arachidonic acid, Linoleic acid, and a-Linolenic acid.
C. Bromine Test for Unsaturation 2. Saturated/Unsaturated 1. Color fades rapidly/persists Fatty acids Stearic acid Oleic acid Triacylglycerols Safflower oil Olive oil Questions and Problems Q3 a. Draw the condensed structural formulas of stearic acid and oleic acid. Stearic acid Oleic acid b. From the results of Part C, which is more unsaturated: oleic acid or stearic a Explain your reason. From the results of Part C, were safflower oil and olive oil saturated or un rated? Explain your reason.
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