
Interpretation:
In each of the given compounds, determine the kind of intermolecular forces existing between their molecules.
Concept introduction:
The attractive forces existing between molecules are said to be intermolecular forces. These forces are the result of mainly three types of interactions:
(a) Dipole–dipole interactions
(b) Dipole–induced dipole interactions
(c) Induced dipole–induced dipole interactions
There are four types of intermolecular forces:
(a) Dispersion forces: These are the intermolecular forces present in all the molecules and atoms by virtue of the electrons present in them.
(b) Dipole–dipole interactions: These are the forces that exist in all polar molecules. They have permanent dipole in which positive end of one permanent dipole is attracted to the negative end of other.
(c) Hydrogen bonding: These forces exist in those molecules having hydrogen atoms bonded directly to the electronegative elements like fluorine, oxygen, or nitrogen.
(d) Ion–dipole forces: Such types of forces exist between the ionic compound molecules.

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Chapter 12 Solutions
Introductory Chemistry (5th Edition) (Standalone Book)
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- Show your work and do something that is reasonable. It does not have to be 100% correct. Just show something that looks good or pretty good as acceptable answers.arrow_forwardShow your work and do something that is reasonable. It does not have to be 100% correct. Just show something that looks good or pretty good as acceptable answers.arrow_forward= 1 = 2 3 4 5 6 ✓ 7 8 ✓ 9 =10 Devise a synthesis to prepare the product from the given starting material. Complete the following reaction scheme. Part 1 of 3 -Br Draw the structure for compound A. Check Step 1 Step 2 A Click and drag to start drawing a structure. × ↓m + OH Save For Later S 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privaarrow_forward
- Predict the products of this organic reduction: 田 Check AP + + H2 Lindlar catalyst Click an drawing 2025 McGraw Hill LLC. All Rigarrow_forward70 Suppose the molecule below is in acidic aqueous solution. Is keto-enol tautomerization possible? • If a keto-enol tautomerization is possible, draw the mechanism for it. Be sure any extra reagents you add to the left-hand sid available in this solution. • If a keto-enol tautomerization is not possible, check the box under the drawing area. : ☐ Add/Remove step Click and drag to st drawing a structure Check Save For Late. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Usearrow_forwardThe problem will not be graded for correctness, but you have to get a reasonable answer something that is either correct or very closer to the correct answer. The instructor professor wants us to do something that shows the answer but everything does not have to be correct. Ideally, yes, it has to be correct. Give it your best shot.arrow_forward
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