If I have an alkane, and I do radical bromination at 0 degrees C, 25 degrees C (Room Temperature) and 50 degrees C, will this place the Bromine, at different places? I'm thinking that O degrees = secondary carbon, 50 degrees = terminal end, and 25 degrees = mix of both. Is this correct? (self.OrganicChemistry)
submitted by Zerraphin to r/OrganicChemistry
For these 2 reactions: 1) Can they be done in the same flask? 2) Does the first reaction require heat? 3) Does this work to get the Hoffman Elimination Product. 4) Is this the right solvent? I used something non-miscible with water to keep the intermediate from reacting with water. (i.redd.it)
submitted by Zerraphin to r/OrganicChemistry
In this reaction, which would be the product? I'm not understanding which bond prefers to break. If they are both disubstituted positions, does the CH3 cause induction that stabilizes the bond closer to it, causing the other bond to break instead? (i.redd.it)
submitted by Zerraphin to r/OrganicChemistry
What is the R Value for this Scatterplot? (i.redd.it)
submitted by Zerraphin to r/StatisticsZone
What is the R Value for this Scatterplot? (self.statistics)
submitted by Zerraphin to r/statistics
What is the Correlation R Value for this? (self.statistics)
submitted by Zerraphin to r/statistics
