1. Represent the movements of the electron pairs and predict the product during the reaction between: 1,3-Butadiene and maleic anhydride: Cyclopentadiene and acrolein (2-propenal):
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- 1. 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.Showusing expanded form the complete halogenation (using Br and UV light) of 2-butyne (2equations). Name your products after the first and second reaction.Compound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yne
- 1. Using Br2 in C2H4Br2 will result in HBr and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. none of the above 2. How many halogenation are posible in propane? a. 3 b. 8 c. 6 d. 10 3.Sulfonation of pentane will result in ________ and water. a. C5H11SO3H b. C5H12SO3H c. C5H14SO3H d. none of the above 4.Nitration of hexane will result in ________ and water. a. C6H13SO3H b. C6H15NO2 c. C6H13NO2 d. C6H14NO2 5.How many moles of O2 in heating a C12H26 (dodecane) a. 27 b. 37 c. 24 d. none of the aboveAnswer all of question 1 pls 1.i. Give two examples each of Unsymmetrical alkenes and reagents.ii. Give two examples of reactions of alkenes that result in Anti-Markonikov’s addition productslab- oxidation of cyclohexene to adipic acid How do you know the products are purified and how is the identity of the product confirmed? Such as if the product is pure, not pure, or not the desired product?
- QUESTION 41,1-dichloroethane is the product of free radical substitution reaction of ethane. Show the overallmechanism including initiation, propagation and termination steps.QUESTION 5a) Cyclopropane exhibit Baeyer’s strain. Explain this statement.b) Compare the reactivity of ring opening reactivity between cyclopropane and cyclobutanebased on the Baeyer’s Strain theory.c) Organized the following cycloalkane in correct order of decreasing stability based onBaeyer strain theory.Cyclopropane, cyclobutane, cyclopentaneSolution:- 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?Proposed chemical reactions which accomplish the objective shown below. Specify reagents, essential conditions and catalysts. A. Convert between cis_alkene to the corresponding trans-allene B. Switch the regiochrmisty of an alkyl halide (example: convert 1 bromopentane to 2-bromopentane
- Hydrogenation of 3-carene (below) can yield two steroisomeric alkane products. Draw their structures. The reaction actually only yields one of the two products. Put a box around the product formed and explain your choice.produce 1,2-Diphenylethene from benzene more than one step may be requiredhelp me please Please fill in the reagents,intermediates, and/or products of the following reactions. all the reactions shall be covered in Chapter 12-15 from Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise.