Trans fatty acids have a higher melting point than their cis isomers because:
a. they are bent due to the trans configuration
b. they contain more carbon atoms
c. they contain fewer carbon atoms
d. the trans configuration affects the pKa of the carboxylic acid group,
e. or of some other reason?
Solution: The correct option is E (or of some other reason?)
The higher melting point of trans fatty acid is due to better packing than cis isomer. The trans isomers pack better than cis isomers because of straighter shape of the chain. The trans fatty acid almost packs like a saturated fatty acid, hence posses higher melting point.
Trans fatty acids have a higher melting point than their cis isomers because: a. they are...
Trans fatty acids have a higher melting point than their cis isomers because: a. they are bent due to the trans configuration b. they contain more carbon atoms c. they contain fewer carbon atoms d. the trans configuration affects the pKa of the carboxylic acid group e. or of some other reason?
Unsaturated fatty acids have lower melting points than saturated fatty acids because A. they have fewer hydrogen atoms B. They have more hydrogen atoms C. their molecules fit closely together D. the cis double bonds give them an irregular shape E. the trans double bonds give them an irregular shape
Unsaturated fatty acids have lower melting points than saturated fatty acids because A. they have fewer hydrogen atoms B. They have more hydrogen atoms C. their molecules fit closely together D. the cis double bonds give them an irregular shape E. the trans double bonds give them an irregular shape
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Which of the following pairs of fatty acids would have the higher melting temperature? 1) C18:0 or C14:0 2) C14:1 or C14:0 3) C16:2 or C20:0 Question 7 1 pts For the triacylglycerol shown, which is the correct description of the middle fatty acid chain? H.C-00 HC-0 H.C-0 ー C18:0 C18 cis-A C18 cis-410 C18 trans- C17:1
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Which of the following explanations describes the fatty acid with the highest melting point: 18 carbons long, 2 double bonds, both in the cis configuration 18 carbons long and saturated 18 carbons long, 1 double bond, cis configuration 18 carbons long, 1 double bond, trans configuration
Carboxylic acids have higher than expected boiling points due to dimeric associations involving hydrogen bonding. The structure of 3-methylbutyric acid is shown below. Draw a second molecule of 3-methylbutyric acid - oriented in the most stable dimeric configuration with the other molecule of acid-and show the intermolecular hydrogen bonds. To indicate a hydrogen bond, draw a regular single bond between the atoms, then click on the "graded select" tool (the yellow highlighter) and click on the bond. A selected bond...