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1. Acetic acid (CH3COOH - though this structural formula does not really show the true connectivity of the atoms) is miscible with water. As more ethylene groups (- CH2-) are added to the middle of the molecule (CH3(CH2),COOH, where n is zero for acetic acid), that is, as n increases, would the molecule become more or less soluble in water? Give an explanation that involves intermolecular forces. add more of The molecule become less soluble in water because if we ethylene group on carboxyl acid the solubity decreases, because the number of carbon and hydrogen atom increase the size of the non polar alkyl group increas that the molecule become hydrophobic, and the solubil.

1. Acetic acid (CH3COOH - though this structural formula does not really show the true connectivity of the atoms) is miscible with water. As more ethylene groups (- CH2-) are added to the middle of the molecule (CH3(CH2),COOH, where n is zero for acetic acid), that is, as n increases, would the molecule become more or less soluble in water? Give an explanation that involves intermolecular forces. add more of The molecule become less soluble in water because if we ethylene group on carboxyl acid the solubity decreases, because the number of carbon and hydrogen atom increase the size of the non polar alkyl group increas that the molecule become hydrophobic, and the solubil.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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NOTE:(I really did want you to state what IMFs exist between the acetic acid and water, and what happens to the number of them as the acid hydrocarbon chain grows, and that effect on solubility.)

1. Acetic acid (CH3COOH - though this structural formula does not really show the true connectivity of the atoms) is miscible with water. As more ethylene groups (- CH2-) are added to the middle of the molecule (CH3(CH2),COOH, where n is zero for acetic acid), that is, as n increases, would the molecule become more or less soluble in water? Give an explanation that involves intermolecular forces. add more of The molecule become less soluble in water because if we octhylene group on carboxyl acid the solubity decreases, because the number of carbon and hydrogen atom increase the size of the non polar alkyl group increas, for that the molecule become hydrophobic, and the solubility of the acid decreases.
Transcribed Image Text:1. Acetic acid (CH3COOH - though this structural formula does not really show the true connectivity of the atoms) is miscible with water. As more ethylene groups (- CH2-) are added to the middle of the molecule (CH3(CH2),COOH, where n is zero for acetic acid), that is, as n increases, would the molecule become more or less soluble in water? Give an explanation that involves intermolecular forces. add more of The molecule become less soluble in water because if we octhylene group on carboxyl acid the solubity decreases, because the number of carbon and hydrogen atom increase the size of the non polar alkyl group increas, for that the molecule become hydrophobic, and the solubility of the acid decreases.
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