![]() They have a similar structure and only differ in that one of the carbon atoms is replaced by an oxygen. Let’s shown this with an example of common organic solvent acetone:Īnd now let’s compare the boiling points of Isobutylene and acetone. And this means, despite being weak, dipole-dipole interactions contribute significantly to the physical properties of compounds when thousands or millions of molecules chain together through this electrostatic iteration. However, in reality, we never deal with two or three molecules, but rather we work in the mole scale. Dipole-dipole interactions are not so strong ( weaker than ionic and covalent bonding). Let’s first discuss the effect of dipole-dipole interactions on the boiling point of organic covalent compounds. Now, to turn into the gas phase, the molecules should overcome the intermolecular interactions and escape the liquid surface, and the stronger these interactions, the harder it is for the molecules to overcome those. In a simpler perspective let’s say that it is the temperature when the liquid turns into a gas even though this process can occur at a large scale of temperature and pressure combination. In other words, we can say it is the temperature at which there is so much of the compound evaporated that it creates a pressure equal to the external pressure. The definition of boiling point states that it is the temperature when the vapor pressure of the compound equals to the atmospheric pressure. We mentioned in the previous post that stronger intermolecular interactions increase the boiling and melting points, but how exactly they affect the physical properties, might be your next question. These, however, are not so relevant in organic chemistry, and therefore, we won’t focus on them as much in this article.īoiling Point and Dipole-Dipole Interactions The ionic bonding is the strongest intermolecular interaction characteristic for inorganic compounds which, as a result, have very high melting points. We will discuss the strength and effect of each interaction typical for covalent compounds below. ![]() In general, for compounds of approximately the same molecular mass, you can follow this trend for the strength of intermolecular interactions: Let’s put the relative strength of intermolecular interactions right before we started. We discussed these infractions in the previous post and today, the focus will be more from the perspective of physical properties. In this post, we will talk about the melting and boiling points of organic compounds and their correlation with intermolecular forces such as dipole-dipole, London dispersion (also known as Van der Waals) interactions, and hydrogen bonding.
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