Which of the following will give a negative test when treated with bromine in carbon tetrachloride? a. 2-Butene b. 2-Butyne с. Butane 1,3-Butadiene
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- In which of the statements given below, the event is not an oxidation reaction? A. Reaction of an alkyl halide with ammonia 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. Formation of the product as a result of the reaction of benzoine with nitric acid E. CH3CH2OH + KMnO4 ® CH3COOHChemistry Please answer the following two questions. 1.) Why are functional group interconversions controversial? (double bonds into epoxide) 2.) Explain the clincal trials that happen for epoxide containing moleculesWhat is the structure of the principal organic product formed in the reaction of 1-iodopropane with NaSH?
- Disiamylborane adds only once to alkynes by virtue of its two bulky secondary isoamylgroups. Disiamylborane is prepared by the reaction of BH3 # THF with an alkene.(a) Draw the structural formulas of the reagents and the products in the preparation ofdisiamylborane.(b) Explain why the reaction in part (a) goes only as far as the dialkylborane. Why isSia3B not formed?what is the best way to come up with how to synthesize carboxylic acid , oct-4-yne to butanoic acid, or trans cyclodecene to decanedoic acid . I keep getting confused on how to go from the reactants to product, even with the amines. i can't figure out what to use to get to the product. Please explain Grignard rx as well.Ethanol, isopropyl alcohol, and n-propyl alcohol may all be used as ingredients in hand sanitizer. Which of those three could be made most easily by reduction of acetone (CHCOCH3) with a hydride reagent?
- 1. In the reactions involving the three isomeric alcohols with the formula C4H9OH, describewhat each of the following tests showed about reactivity of the -OH group and reactions of 1°,2°, and 3° alcohols.• the test with neutral KMnO4• the test with concentrated HCl2. Predict how the fourth alcohol with the formula C4H10O would react if tested with:• 0.01 M KMnO4• concentrated HCl at room temperatureExtend FurtherUse your observations of the solutions formed in the previous experiments and yourunderstanding of alcohols to complete a table like the one shown below. Research the meltingand boiling points to verify your answers.What does alkyl halides gives on heating with dry Ag2O ?Oxidation of a primary alcohol with pyridinium chlorochromate ( PCC, C5H6NCrO3Cl) would yield what?
- What is the monomer used to prepareOne of the earliest commercial plastics was Bakelite®, formed by the reaction of phenol with a little more than one equivalent of formaldehyde under acidic or basic conditions. Baeyer first discovered this reaction in 1872, and practical methods for casting and molding Bakelite were developed around 1909. Phenol-formaldehyde plastics and resins (also called phenolics) are highly cross-linked because each phenol ring has three sites (two ortho and one para) that can be linked by condensation with formaldehyde. Suggest a general structure for a phenol-formaldehyde resin, and propose a mechanism for its formation under acidic conditions.Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the presence of H2SO4 and provide a clear rationale as to why this is the major product of the reaction and the minor product of the reaction.