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Molar Mass Of Gas Essay



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Practice Problem: Molar Mass of a Gas

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Alkanes: "Alkanes have low reactivity and undergo free-radical substitution reactions. Bromine water can be used to distinguish between alkenes and alkanes. They can undergo nucleophilic substitution reactions. A nucleophile is an electron-rich species containing a lone pair that it donates to an electron-deficient carbon. The FC is the charge an atom would have if all atoms in the molecule had the same electronegativity. The Lewis electron dot structure with the atoms having FC values closest to zero is preferred. A resonance structure is one of two or more alternative Lewis electron dot structures for a molecule or ion that cannot be described fully with one Lewis electron dot structure alone.

The more ways the energy can be distributed the higher the entropy. The order of a reaction can describe, with respect to a reactant, the number of particles taking part in the rate-determining step. Solute concentration is 1 mol dm-3 or kPa for gases. Nucleophilic Substitution Reactions: "SN1 represents a nucleophilic unimolecular substitution reaction and SN2 represents a nucleophilic bimolecular substitution reaction. SN1 involves a carbocation intermediate. SN2 involves a concerted reaction with a transition state. Both mechanisms occur for secondary halogenoalkanes.

SN2 is stereospecific with an inversion of configuration at the carbon. Electrophiles are Lewis acids. The formation of the major product can be explained in terms of the relative stability of possible carbocations in the reaction mechanism. Each carbon to carbon bond has a bond order of 1. Benzene is susceptible to attack by electrophiles. Ketones can be reduced to secondary alcohols. Typical reducing agents are lithium aluminium hydride used to reduce carboxylic acids and sodium borohydride. Functional group interconversions are the basis of such synthetic routes.

Optical isomers are enantiomers. Enantiomers are non-superimposeable mirror images of each other. Diastereomers are not mirror images of each other. Self-assembly can also occur spontaneously in solution. The hydrogen bonds between O and N can be broken with the use of concentrated sulfuric acid. Proteins and enzymes. Fatty acids can be saturated, monounsaturated or polyunsaturated. Their specific colour depends on metal ions and pH. They are susceptible to oxidation, catalysed by light. Energy and materials go from a concentrated into a dispersed form. The quantity of the energy available for doing work decreases.

Non-renewable energy sources are finite. The different fractions are separated by a physical process in fractional distillation. It is generally expressed in equivalent tons of carbon dioxide. You need to do plenty of practice problems to feel comfortable with the material, and, if you cram, you won't be able to spend enough time on this. Don't pull out your notes the day before the exam and expect to learn everything in one marathon study session.

You won't retain the information, and you'll be exhausted for the test. C ramming is a lot like trying to hold a huge volume of water back with a really flimsy dam. It's not gonna work out well. The notes in this article should help you review all the essential concepts you need to know for the AP Chemistry exam. Make sure you supplement your review with practice tests so you can assess your progress and see where your main strengths and weaknesses lie.

Also, keep in mind the tips I went through in the last section:. Do you need notes for additional AP classes besides Chemistry? Notes are all well and good, but when do you actually need to start using them to review for the test? Find out how early you should start studying for AP exams if you're aiming for a great score. Have you planned out your schedule for the rest of your time in high school yet? If not, t his guide will help you decide which AP classes to take in the future!

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