The main Organic Chemistry 1 chapters in most US curricula go up to the reactions of alcohols. So, this summary will include synthesis practice problems on Alkenes, Alkynes, and Alcohols. If you need to practice SN1, SN2, E1, and E2 … Read more
In the previous post, we saw that ozonolysis is used to convert alkenes into aldehydes and ketones through the oxidative cleavage of the C=C double bond. Here are some ozonolysis practice problems for alkenes and alkynes, where you … Read more
Have you seen your professor talking about BH₃ and H₂O₂ and not quite understood what it is and when to use it?Ok, so, keeping it simple, we use BH₃ together with a peroxide to place an OH group on the … Read more
Alkenes react at low temperatures with either pure liquid bromine or a bromine solution in an organic solvent such as tetrachloromethane. During the reaction, the double bond breaks, and each carbon atom gains a bromine atom, forming a vicinal dibromide: … Read more
Halonium ions are structures where a halogen atom is connected to two alkyl groups: In your organic chemistry class, you are only going to worry about a specific type of halonium ion where the halogen is part of … Read more
This content is for registered users only. Click here to Register! By joining Chemistry Steps, you will gain instant access to the answers and solutions for all the Practice Problems, including over 40 hours of problem-solving videos, Multiple-Choice Quizzes, Puzzles, Reaction … Read more
There are direct ways of converting alkenes to amines covered in undergraduate organic chemistry textbooks, so a question like this is most likely meant to test your knowledge on multiple functional group transformations. The strategy here is to … Read more
Alkenes are converted to alkyl halides by the addition reactions of hydrohalic acids (HCl, HBr, HI). These are generally Markovnikov additions unless we direct the Br to the less substituted carbon atom radical addition using a peroxide catalyst: From reaction … Read more
Let’s discuss a few strategies for converting alkenes to carboxylic acids that allow to increase the length of the carbon chain, decrease it, and keep it the same as well: Alkenes to Carboxylic Acids: Keeping the Length of … Read more
Markovnikov’s rule is a general trend predicting that in the reactions of HX (HCl, HBr, HI) species with unsymmetrical alkenes, the X adds to the more substituted carbon of the double bond. The reason for this is the greater stability … Read more
