Editing 2943: Unsolved Chemistry Problems

Jump to: navigation, search

Warning: You are not logged in. Your IP address will be publicly visible if you make any edits. If you log in or create an account, your edits will be attributed to your username, along with other benefits.

The edit can be undone. Please check the comparison below to verify that this is what you want to do, and then save the changes below to finish undoing the edit.
Latest revision Your text
Line 12: Line 12:
 
{{incomplete|Created by a caffeinated biochemist - Please change this comment when editing this page. Do NOT delete this tag too soon.}}
 
{{incomplete|Created by a caffeinated biochemist - Please change this comment when editing this page. Do NOT delete this tag too soon.}}
  
Every field of research has [[:Category:Incomplete explanations|unsolved problems]] considered "important" or "significant" that motivate continued research. The scientists at what is apparently the "grand opening" of their new chemistry lab list several real chemistry problems, followed by one also-unsolved-but-less-scientific problem (the p in pH)  
+
There is a list of mathematical problems that are yet to be solved (such as P=NP). This comic makes a spin on it, by stating that there are (as of yet) unsolved chemistry problems. The scientist at what is apparently the "grand opening" of a new chemistry lab lists several real chemistry problems, followed by one also-unsolved-but-less-scientific problem (the p in pH)  
  
 
'''Arbitrary Enzyme Design:'''  
 
'''Arbitrary Enzyme Design:'''  
  
{{w|Enzymes}} are catalytic proteins. Enzyme catalysis is often unique in comparison with other catalysis methods as it is highly specific, or tailored to a specific reaction. As such, enzyme catalysis, besides being the basis of all biochemical processes, is becoming increasingly relevant to industrial synthesis processes. As enzymes can easily be produced synthetically through recombinant gene technology, being able to design an arbitrary enzyme for any reaction would mean that effectively any reaction could be relatively easily catalyzed, revolutionizing the chemical synthesis industry.
+
{{w|Enzymes}} are catalytic proteins. Enzyme catalysis is often unique in comparison with other catalysis methods as it is highly specific, or tailored to a specific reaction. As such, enzyme catalysis, besides being the basis of all biochemical processes, is becoming increasing relevant to industrial synthesis processes. As enzymes can be easily synthetically produced through recombinant gene technology, being able to design an arbitrary enzyme for any reaction means that effectively any reaction can be relatively easily catalyzed, revolutionizing the chemical synthesis industry.
  
 
'''Protein Folding:'''   
 
'''Protein Folding:'''   
  
{{w|Protein|Proteins}} are large molecules that consist of chains of amino acids.  These amino acid chains become {{w|Protein Folding|folded}} in extremely complex ways to form intricate 3D structures, and the way a protein is folded is of critical importance to its function. Because of the huge importance of proteins to biological life, biologists have devoted significant attention over many decades to the problem of {{w|Protein structure prediction|protein structure prediction}}. This refers to the ability to predict the 3D structure of a protein based on the amino acid sequence, and remains one of the most important problems in computational biology. The ability to predict protein structure purely from amino acid sequence the so-called "de novo" prediction is known in computational biology as an unusually difficult problem due to the complexity of amino acid chains. Known as "Levinthal's paradox," the number of possible conformations from the backbone conformations alone is estimated to be in the ballpark of 10^300. Despite this, protein folding occurs extremely quickly in reality. Because of this difficulty in sampling conformations, even with optimization, such as secondary structure prediction and Monte Carlo simulation, a "true" accurate simulation is extremely computationally expensive. Because of this, the most accurate solutions, such as AlphaFold, utilize a combination of homology modeling (sampling experimentally determined proteins with similar sequences to infer structural motifs and similarities) and deep learning to accurately guess protein structure. See also [[1430: Proteins]].
+
{{w|Protein|Proteins}} are large molecules that consist of chains of amino acids.  These amino acids chains become {{w|Protein Folding|folded}} in extremely complex ways into intricate 3D structures, and the way a protein is folded is of critical importance to its function. Because of the huge importance of proteins to biological life, biologists have devoted significant attention over many decades to the problem of {{w|Protein structure prediction|protein structure prediction}}. This refers to the ability to predict the 3D structure of a protein based on the amino acid sequence, and remains one of the most important problems in computational biology. The ability to predict protein structure purely from amino acid sequence, the so-called "de novo" prediction, is known in computational biology as an unusually difficult problem due to the complexity of amino acid chains. Known as "Levinthal's paradox," the number of possible conformations from the backbone conformations alone is estimated to have in the ballpark of 10^300 different conformations. Despite this, protein folding occurs extremely quickly in reality. Because of this difficulty in sampling conformations, even with optimization, such as secondary structure prediction and Monte Carlo simulation, a "true" accurate simulation is extremely computationally expensive. Because of this, the most accurate solutions, such as AlphaFold, utilize a combination of homology modeling - sampling experimentally determined proteins with similar sequences to infer structural motifs and similarities - and deep learning to accurately guess protein structure.  
  
 
'''Depolymerization:'''
 
'''Depolymerization:'''
  
Polymers are very large molecules formed out of repeating subunits called monomers. Monomers are molecules, typically organic in nature, that can bond with at least one other molecule, with two or more making long chains or networks called polymers. That process is known as polymerization. Depolymerization is breaking polymers down into the small molecules they were originally made from. This is done through a variety of processes, such as radiation, electrolysis, adding chemicals, and other means. Plastics are the best-known polymers, but cellulose, proteins, and DNA are also technically polymers. The huge number of varieties and mixtures in plastics makes recycling them a huge challenge, and there is increasing concern about plastic waste damaging the environment.
+
Polymers are very large molecules formed out of repeating subunits called monomers. Monomers are molecules, typically organic in nature, that can bond with at least 2 other molecules, making long chains or networks. That process is known as polymerization. Depolymerization is breaking down polymers into the small molecules they were originally made from. This is done through a variety of processes such as using radiation, electrolysis, adding chemicals, and other means. Plastics are the best-known polymers, but cellulose, proteins, and DNA are also technically polymers. The huge number of varieties and mixtures in plastics makes recycling them a huge challenge, and there is increasing concern about plastic waste damaging the environment.
  
Polymerization is usually exothermic, releasing energy as heat. To reverse this would require adding energy in a targeted way. Simply ''destroying'' a polymer by means of highly-reactive chemicals, heat, or radiation doesn't generally release the monomer molecules to a significant degree; most of the reaction products are highly degraded. Most polymers are made by a process of catalysis, with the small monomer molecules interacting via a catalyst structure, often in liquid form, and the eventual product is usually solid. To reverse this would require getting the catalyst to interact in a very precise way with the solid polymer, and it's relatively difficult for the catalyst structure to get into the proper configuration with the solid tangled polymer molecules.
+
Polymerization is usually exothermic, releasing energy as heat. To reverse this would require adding energy, in a targeted way. Simply ''destroying'' a polymer, by means of highly-reactive chemicals, heat, or radiation, doesn't generally release the monomer molecules to a significant degree; most of the reaction products are highly degraded. Most polymers are made by a process of catalysis, with the small monomer molecules interacting via a catalyst structure, often in liquid form, and the eventual product is usually solid. To reverse this would require getting the catalyst to interact in a very precise way with the solid polymer, and it's relatively difficult for the catalyst structure to get into the proper configuration with the solid tangled polymer molecules.
  
 
Another highly-desired depolymerization process would be to convert cellulose into its component glucose molecules. That glucose could then be used for a variety of different purposes, including fermentation to alcohol to use as a fuel. Currently, when plants are grown, much of the solar energy and carbon dioxide they absorb ends up in the form of cellulose rather than as starch, sugar, protein, or other substances that we find useful. Our being able to make use of the cellulose would make farming much more energy-efficient. Some organisms are able to depolymerize cellulose by means of enzymes, but our ability to use similar processes on an industrial scale is still limited. (Those organisms use a complex multi-step biochemical process which essentially "invests" energy into splitting off a glucose molecule, then recoups the investment by metabolizing the glucose.) It's also possible to depolymerize cellulose at high temperature and pressure using nothing more than water and acid, but that process is energy-intensive. It ''might'' be possible to do it with a solar-heated reactor.
 
Another highly-desired depolymerization process would be to convert cellulose into its component glucose molecules. That glucose could then be used for a variety of different purposes, including fermentation to alcohol to use as a fuel. Currently, when plants are grown, much of the solar energy and carbon dioxide they absorb ends up in the form of cellulose rather than as starch, sugar, protein, or other substances that we find useful. Our being able to make use of the cellulose would make farming much more energy-efficient. Some organisms are able to depolymerize cellulose by means of enzymes, but our ability to use similar processes on an industrial scale is still limited. (Those organisms use a complex multi-step biochemical process which essentially "invests" energy into splitting off a glucose molecule, then recoups the investment by metabolizing the glucose.) It's also possible to depolymerize cellulose at high temperature and pressure using nothing more than water and acid, but that process is energy-intensive. It ''might'' be possible to do it with a solar-heated reactor.
Line 32: Line 32:
 
'''What the “p” in pH stands for:'''
 
'''What the “p” in pH stands for:'''
  
“p” shows up in pH, pOH, pK<sub>a</sub>, pK<sub>b</sub>, and other things related to the concentration of H+ ions and OH- ions. The meaning of the "p" in "pH" has been the subject of much dispute. It is sometimes referred to as "power of Hydrogen", perhaps related to the fact that pH is a logarithmic scale, and the logarithm is the inverse of the exponented function and, in all three languages that pH was first published in, the word for "potency" is used for exponents. The term pH was introduced by {{w|Søren Peter Lauritz Sørensen|Søren Peter Lauritz Sørensen}}, who did not publish his results in English, and more accurately translates as "hydric exponent". The letter p could stand for, in the languages in which Sørensen published: the French 'puissance', German Potenz, or Danish potens, all referring to the concept of the "exponent" in exponential functions.  
+
“p” shows up in pH, pK<sub>a</sub>, pK<sub>b</sub>, and other things related to the concentration of H+ ions and OH- ions. The meaning of the "p" in "pH" has been the subject of much dispute. It is sometimes referred to as "power of Hydrogen", but it's not at all clear in English what this means - are we talking about hydrogen fuel cells, or someone's superpower? The connection - which most teachers (original research) do not make - is that this "power" should be understood in the sense of "x to the third power." pH is a logarithmic scale, and the logarithm is the inverse of the exponent, and, in all three languages that pH was first published in, the word for "potency" is used for exponents. The term pH was introduced by {{w|Søren Peter Lauritz Sørensen|Søren Peter Lauritz Sørensen}}, who did not publish his results in English, and more accurately translates as "hydric exponent". The letter p could stand for,in the languages in which Sørensen published: the French 'puissance' , German Potenz, or Danish potens, all referring to the concept of the "exponent" in exponential functions.  
  
 
'''Title Text: Hydrogen Denier'''
 
'''Title Text: Hydrogen Denier'''
Line 40: Line 40:
 
Here's a breakdown of this joke:
 
Here's a breakdown of this joke:
  
* H<sup>+</sup> is the chemical symbol for a positively-charged atom of hydrogen, the smallest atom on the Periodic Table. Since hydrogen is normally just one proton and one electron, when you take the electron away, you make it positively charged (the + sign in the superscript) and you effectively end up with just a single loose proton. So the shorthand for "loose proton" is to refer to it as an H<sup>+</sup> ion.
+
* H<sup>+</sup> is the chemical symbol for a positively-charged atom of hydrogen, the smallest atom on the Periodic Table. Since hydrogen is normally just one proton and one electron, when you take the electron away, you make it positively charged (the + sign in the superscript) and you effecitvely end up with just a single loose proton. So the shorthand for "loose proton" is to refer to it as an H<sup>+</sup> ion.
  
* pH is taught in high school science class to essentially measure the concentration of extra loose protons in, say, an aquarium. (Different fish prefer slightly different pH levels/alkalinity.) As mentioned earlier, you can interpret the term "pH" to be referring to the "p" of "H" -- the power/potency of H<sup>+</sup> ions.
+
* pH is taught in high school science class to essentially measure the concentration of extra loose protons in, say, an aquarium. (Different fish prefer slightly different pH levels/alkilinity.) As mentioned earlier, you can interpret the term "pH" to be referring to the "p" of "H" -- the power/potency of H<sup>+</sup> ions.
  
(Note that in reality, lone H+ ions do not exist in water, and instead they glom onto H<sub>2</sub>O molecules to form H<sub>3</sub>O<sup>+</sup> and H<sub>5</sub>O<sub>2</sub><sup>+</sup>/(H<sub>2</sub>O--H--OH<sub>2</sub>)<sup>+</sup> due to intermolecular hydrogen bonding. If you don't know what these chemical symbols mean, don't worry about it.)
+
(Note that in reality, lone H+ ions do not exist in water, and instead they glom onto H2O molecules to form H3O+ and H5O2+/(H2O--H--OH2)+. If you don't know what these chemical symbols mean, don't worry about it.)
  
But as an H<sup>+</sup> denier, Randall doesn't consider loose protons to be hydrogen atoms. He has a purist's view of hydrogen, that it is just "pretending" to be hydrogen as soon as it loses an electron. As a denier, he interprets the term "pH" as referring to the concentration of "pretend Hydrogen".
+
But as an H<sup>+</sup> denier, Randall doesn't consider loose protons to be hydrogen atoms. He has a purist's view of hydrogen, that it is just "pretending" to be hydrogen as soon as it loses an electron. As a denier, he interprets the term "pH" as referring to the concentration of "pretend Hyodrgen."
  
 
==Transcript==
 
==Transcript==
Line 59: Line 59:
 
[[Category:Comics featuring Cueball]]
 
[[Category:Comics featuring Cueball]]
 
[[Category:Comics featuring Megan]]
 
[[Category:Comics featuring Megan]]
[[Category:Comics with lowercase text]]
 
 
[[Category:Multiple Cueballs]]
 
[[Category:Multiple Cueballs]]
 
[[Category:Chemistry]]
 
[[Category:Chemistry]]

Please note that all contributions to explain xkcd may be edited, altered, or removed by other contributors. If you do not want your writing to be edited mercilessly, then do not submit it here.
You are also promising us that you wrote this yourself, or copied it from a public domain or similar free resource (see explain xkcd:Copyrights for details). Do not submit copyrighted work without permission!

To protect the wiki against automated edit spam, we kindly ask you to solve the following CAPTCHA:

Cancel | Editing help (opens in new window)