…it comes to exam time. Just remember this: Protonation / 1,2-Addition / Proton transfer / 1,2-Elimination / Deprotonation. PAPED. I’ve been trying to come up with a good mnemonic for…
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…the course, because this is the level of understanding that is generally tested for on exams. Here are some examples of general questions that reflect a more conceptual understanding of…
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…of chain Suffix = highest priority functional group And so your simple approach is as follows: When you come across a complex molecule with multiple components to name, identify each…
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…brought to the exam. Look at this example. Using a line drawing or a Fischer projection to make a model is relatively straightfoward. Therefore, with the assistance of a model,…
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…synthetic standpoint!]. You might recall there are two important free-radical halogenation reactions of alkanes: free radical chlorination, and free-radical bromination. Table of Contents Free-Radical Chlorination of Alkanes Free-Radical Bromination of…
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…stereochemistry – “geometric isomers” (e.g. cis/trans isomers in cycloalkanes and alkenes) being the prime example. Level 4– Now comes the chapter on stereochemistry, which is probably the key theme of…
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…Do you have an exam on alkene and alkynes coming up? We went through hundreds of exams and hand-picked the most “classic” types of questions you’re likely to see on…
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…how can the sequence alkane –> alkyl halide –> alkene –> alkane be accomplished? Feel free to post your answers in the comments below! 4. Combined Reaction Map: Reactions of…
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…material and product, what reagents are required? Given the reagents and the product, what starting material is required? You’ll notice that these are very common exam-type questions. If you have…
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…have locator for all substituents. Example: 1,1-dimethyl is correct. 1-dimethyl is incorrect. 1,1-methyl is incorrect. These are common mistakes. F. Branched substituents are numbered and named seperately from the main…
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