WebbHIO4, H2O, THF What is the best choice of reagent (s) to perform the following transformation? 1, poly (vinyl acetate); 2, poly (methyl methacrylate); 3, polystyrene; 4, … WebbDMSO or THF (solvent) (2. H2O (Aqueous workup)) Mix Reactants in Alcohol (solvent) HF (catalyst) (catalyst) (catalyst) (cold, dilute) (hot, dilute) (cool, concentrated) (heated, concentrated) NaOH: HOEt, 25 o C: NaH: NaNH2: THF, -78 o C: 1. BH3/THF 2. HO-, H2O2, H2O: HBr: HBr ROOR, Light: Br2 CCl4: Br2 H2O: Br2 H3O+ (Acetic Acid) Br2 …
Answered: 9. Of the compounds below, which is… bartleby
WebbOrganic Chemistry Reactions of Alkynes. Alkynes have a very similar reactivity to alkenes. They undergo the electrophilic additions like halogenation and hydrohalogenation. They can also be reduced with the aid of a heterogeneous catalyst or oxidized via several techniques. Alkynes do, however, have a number of unique reactions that you’re ... WebbTo find the correct oxidation state of I in HIO4 (Periodic acid), and each element in the compound, we use a few rules and some simple math. First, since the HIO4 doesn’t have an overall charge ... jazan group
Periodic acid - Wikipedia
WebbPeriodic acid is the highest oxoacid of iodine, in which the iodine exists in oxidation state VII. Like all periodates it can exist in two forms: orthoperiodic acid, with the chemical formula H 5 IO 6 and metaperiodic acid, which has the formula HIO 4. Periodic acid was discovered by Heinrich Gustav Magnus and C. F. Ammermüller in 1833. WebbConsider the reactions.a) CH3 - CH = CH2 [ (ii)H2O/OH] (i)BH3/THF A [ (in CH2Cl2)]PCC B b) CH3 - CH = CH2 [ (ii)NaBH4 O̅H] (i)Hg (OAc)2 C [ (in CH2Cl2)]PCC D Product B and D are: Class 12 >> Chemistry >> Aldehydes, Ketones and Carboxylic Acids >> Preparation of Aldehydes and Ketones >> Consider the reactions.a) CH3 - CH = CH2 Question Webb1. KMnO4, NaOH. 2. H3O+. Note: Similar oxidative function of chromic acids, except done under basic conditions. Note: PCC oxidizes primary alcohols to aldehydes, not carboxylic acids. Note: Periodic acid can cleave glycols (1,2 diols) into respective carbonyls. 1. jazan area