Q3// When oxidation of 2-methtyl-2-butene with hot potassium permanganate in alkaline medium from sodium hvdroxide the products presence ketones and organic acid ? Writ the chemical reaction and write the name for all compounds?
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- find the carboxylic acid that cab ve oreoared from 4-bromomethylbenzenea. by direct oxidationb. by free radical chlorination followed by nitrile synthesisshowed the synthesis of dec-3-yne by adding the hexyl groupfirst, then the ethyl group. Show the reagents and intermediates involved in theother order of synthesis of dec-3-yne, by adding the ethyl group first and the hexylgroup last.Solution:- 3. Determine the amount, in of a (2.20 M s olution of dichloromethane needed to completely react with 15.72g cyclohexene to give 1,2-dibromocuclohexanw. Assume 12% excess is needed in order to react completely. a . How much 1,2 -dibromocyclohexane would theoretically be produced ? c. How many ML of the 2.20 M Br2 solution are required?
- What is the experimental yield (grams and percentage) Experiment: Oxidation of -Chlorotoluene to o-Chlorobenzoic acid materials used dissolved 3.35 g of KMnO4 1.20 mL of 2-chlorotoluene was added to the mixture 3.0 mL of concentrated hydrochloric acid (pH~2) 10 mL of toluene -The crystals were isolated by vacuum filtration- Product Characterization 1.15 g of the crude product 0.93 g of the final product M.p. (final): 139-141 oC1. Write down all the steps of the reaction of 2-Methyl-2-hexene with sulfuric acid and name the product formed. Will provide helpful ratings for correct solution.Represent the reaction equation of the alkene supplied to you with propanol, in acidic medium, indicating thestereochemistry of all the products formed.
- One possible way of determining the identity of an alkene, is to let itundergo an oxidative cleavage reaction in the presence of hot basicpotassium permanganate. You are given two containers said to containdifferent alkenes. Container A is marked as cis / trans‐2‐butene andcontainer B as 2‐methyl‐1‐butene. Explain by referring to the formation ofproducts, how you would verify the identity of the alkenes.In which of the statements given below, the event is not an oxidation reaction? A. Product formation as a result of the reaction of benzoine with nitric acid B. Formation of the product as a result of the reaction of 2-propene at KMnO4 / Basic ambient temperature C. Formation of the product as a result of the reaction of 2-propene in KMnO4 / Basic medium cold D. CH3CH2OH + KMnO4 → CH3COOH E. Reaction of an alkyl halide with ammoniaWhat prpduct would you expect from the reaction of cyclopentene with NBS and water? show the stereochemistry? Please draw up the reaction and all the chemistry formed.
- An alkene with molecular formula C8H16 was obtained from ozonolysisreaction and give acetone and 2,2-dimethylpropanal as the product. Writethe chemical equation from the reactionCompound K, L and M are three isomers with the molecular formula C5H10O.Compound K cannot be oxidized, while compound M and L can be oxidized.Oxidation of compound L with hot acidified potassium permanganate,KMnO4 solution yields 2-methylbutanoic acid. When treated with Iodoformreagent, yellow precipitation only occurs in compound K. Fehling test onlyyielded positive results for compound L and negative for compound M andK. Compound M is then reacted with hydrogen chloride, HCl produceschlorocyclopentaneCompound K, L and M are three isomers with the molecular formula C5H10O.Compound K cannot be oxidized, while compound M and L can be oxidized.Oxidation of compound L with hot acidified potassium permanganate,KMnO4 solution yields 2-methylbutanoic acid. When treated with Iodoformreagent, yellow precipitation only occurs in compound K. Fehling test onlyyielded positive results for compound L and negative for compound M andK. Compound M is then reacted with hydrogen chloride, HCl produceschlorocyclopentane (i) Draw the structural formula of compounds K, L and M.