Since we’re comparing methylamine to the amino group on the amino acid, we’re only interested in its ability to accept a proton and form a conjugate acid. ![]() Methylamine is amphiprotic, meaning that it can donate or accept a proton thus acting as an acid or a base. Now let’s take a look at a simple base like methylamine. That’s where my Henderson Hasselbalch trick comes in handy, as explained in the video below. You REALLY don’t want to waste time with calculations like this on the MCAT. ![]() Using the Henderson-Hasselbalch equation for buffers, it’s possible to calculate the pH based on the ratio of acid to conjugate base, or calculate the ratio given the pH and pKa value. Since acetic acid is considered a weak acid (strong within the scale of weak acids), there is a range at which the acetic acid and acetate will form a stable buffer. What is the turning point of this equilibrium? As the pH increases, equilibrium will continue to shift to the right, favoring the deprotonated acetate form over the protonated acetic acid. Since the OH- will react with the free H+ in solution to form water, Le Chatelier’s principle says the reaction must shift to the right to reform that H+. The reaction now favors the protonated acetic acid form.Īs the pH is increased with the addition of a strong base like sodium hydroxide (NaOH), the equilibrium will now shift to the right. According to Le Chatelier’s principle, if product is added, the system will shift to the left to reestablish equilibrium. These free H+ ions will protonate any free acetate ions in solutions thus favoring the product of this equilibrium reaction. If we lower the pH of a solution by adding a strong acid like HCl, there will be an abundance of H+ in the solution. Disregard the complex ICE charts for calculating dissociation instead, look at what drives this reaction towards the right or left. If you find your acid/base knowledge weak, start by reviewing my acid/base video series, reading this (link) acid/base overview article, and downloading my free acid/base cheat sheet.Ī carboxylic acid in solution will exist in equilibrium with carboxylate or acetate, its conjugate base. Let’s compare the carboxyl and amine groups to simple molecules like acetic acid and methyl amine. (Learn more about amino acid side chains link) Finding Charge on a Carboxyl Group Acidic and basic amino acids may have additional groups in their side chains. The standard structure contains both a carboxyl and an amine in the backbone. This is the zwitterion form of an amino acid While neutral, the zwitterion form of an amino acid will have a positive and a negative charge. Zwitterion comes from the German word for ‘two’ (zwei) or ‘double’ (zwitter) and the word ‘ion’. That’s not because they have no charge: it’s because their charges balance or cancel out. This drawing is simplified, and is actually incorrect.Īt physiological pH, amino acids will exist with a net charge of zero. Looking at this standard drawing of an amino acid, it appears to be neutral–how does that relate to the pl? The isoelectric point or pI of an amino acid is the pH at which an amino acid has a net charge of zero. The word isoelectric or isoelectronic comes from ‘iso,’ which means the same, and ‘electric,’ which implies charge. When you think of amino acid charge, the first related topic that comes to mind is isoelectric point. While the math concept may be tricky at first, you’ll find that once it makes sense, it’s fairly easy to apply these critical skills for the MCAT. The MCAT is a test of logic and understanding, which is why this article will break down amino acid charge and calculations from a logical application perspective. Understanding why an amino acid will gain or lose a proton at a given pH is even more critical. Knowing how to find both charge and isoelectric point for amino acids is a critical MCAT skill.
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