Tutorial:Basic Chemistry Topics: Difference between revisions

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'''Essential vs. Nonessentail Amino Aicds'''
'''Essential vs. Nonessentail Amino Aicds'''


An amino acid is considered essential when the human body is not capable of synthesizing/producing it. These amino acids need to be obtained from our diet. If the body is capable of producing an amino acid through metabolism or another method, the amino acid is classified as nonessential.
An amino acid is considered essential when the human body is not capable of synthesizing/producing it. These amino acids need to be obtained from our diet. If the body is capable of producing an amino acid through metabolism or another method, the amino acid is classified as nonessential.  
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''Essential Amino Acids''
''Essential Amino Acids''
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'''Neutral, Polar vs. Nonpolar Amino Acids'''
'''Neutral, Polar vs. Nonpolar Amino Acids'''


The polarity of an amino acid is dependent on the difference in electronegativity and the asymmetry of the compounds structure, discussed previously. For example, Arginine is a polar amino acid and Glycine is a nonpolar amino acid. As we learned earlier, an amino acid structure consists of a carboxylic acid, an amine, hydrogen, and a functional group. Look at the structure of arginine; the amine group, carboxylic acid and hydrogen are located towards the bottom of the representation. The functional group is the large extension of atoms upward. You can see from this image that the functional group has a greater density/electronegativity compared to the rest of the structure, hence making this amino acid polar. In contrast the structure of glycine, located next to arginine, has little polarity. The functional group attached is only a methyl group (CH3), which has low density/electronegativity compared to the rest of the structure making glycine a nonpolar amino acid. Neutral amino acids have functional groups that are similar in electronegativity, so the electrons are not pulled in one direction more dominantly then another. In other words, there is no increase in density to one side. When an amino acid is neutral, it is less reactive then a polar amino acid. It is less reactive because the structure is stable. A polar amino acid is pulling electrons yielding a slight positive and negative charge with in the amino acid structure, making it less stable. Those charges want to react with other atoms, yielding the higher reactivity.  
The polarity of an amino acid is dependent on the difference in electronegativity and the asymmetry of the compounds structure, discussed previously. For example, Arginine is a polar amino acid and Glycine is a nonpolar amino acid. As we learned earlier, an amino acid’s structure consists of a carboxylic acid, an amine, hydrogen, and a functional group. Look at the structures of <scene name='Tutorial:Basic_Chemistry_Topics/Polar_nonpolaraa/1'>arginine and glycine</scene>. Arginine has the amine group, carboxylic acid and hydrogen located towards the bottom of the representation, and the functional group is the large extension of atoms upward. You can see from this image that the functional group has a greater density/electronegativity compared to the core of the amino acid (carboxylic acid, amine and hydrogen), hence making this amino acid polar. In contrast the structure of glycine, located next to arginine, has little polarity. The functional group attached to glycine is only a methyl group (CH3). A methyl group has low density/electronegativity compared to the rest of the structure, making glycine a nonpolar amino acid. Neutral amino acids have functional groups that are similar in electronegativity compared to the core, so the electrons are not pulled in one direction more dominantly then another. In other words, there is no increase in density to one side. When an amino acid is neutral, it is less reactive then a polar amino acid. It is less reactive because the structure is stable. A polar amino acid is pulling electrons yielding a slight positive and negative charge within the amino acid structure, making it less stable. Those charges want to react with other atoms, yielding the higher reactivity.  
<scene name='Tutorial:Basic_Chemistry_Topics/Polar_nonpolaraa/1'>Arg/Gly</scene>
<scene name='Tutorial:Basic_Chemistry_Topics/Polar_nonpolaraa/1'>Arg/Gly</scene>
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