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- b. Increasing reactivity with HBr H3C Н H3C A Н least reactive н н Н В I H3C Н C I н н Н D CH₂CH3 most reactive2. Explain the selectivity of the following reaction, which produces a single product despite both alkene carbons being equally substituted. H3C CF3 HBr CF3 H3C CF3 H3C Br- H3C only product -H CF3What is the major organic product of the following reaction? Br₂ SH آمديد مياده مبار Br || SH III IV
- Consider the reaction scheme below. Br2 FeBr3 AICI3 NaOH warm What are the structures of X, Y, and Z? Include all possible substitution productsAlcohols are important for organic synthesis, especially in situations involving alkenes. The alcohol might be the desired product, or the OH group might be transformed into another functional group via halogenation, oxidation, or perhaps conversion to a sulfonic ester derivative. Formation of an alcohol from an alkene is particularly powerful because conditions can be chosen to produce either the Markovnikov or non-Markovnikov product from an unsymmetrical alkene. Using your reaction roadmap as a guide, show how to convert 4-methyl-1-pentene into 5-methylhexanenitrile. You must use 4-methyl-1-pentene and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.Which is true of a free energy diagram for an SN1 eaction? It shows one transition state. It always shows that the reaction is net exothermic. It never shows intermediates. It always shows that the reaction is net endothermic. It always includes multiple energy barriers.
- What is the major substitution product to the following reaction? Но OCH,CH3 Chapter 9 Homew..pdf IMG_4217 (1)jpeg MG 4217jpeg INSubstitution and Elimination (Please draw the structures involved in the reactions) A. Which will react more rapidly via SN1? 1-bromo-2,2-dimethylpropane or 2-bromo-2- methylbutane? Explain. B. Which will react faster via SN2? 1-chlorocyclohexane or 1-chloro-1-methylcyclohexane? Explain.Organic Chemistry Indicate which carbocation is the most stable carbocation and which carbocation is the least stable carbocation?Çok Satırlı Metin.
- How many stereoisomers are formed in the reaction below? Please note: both alkenes will react under these conditions. 1. Hg(OAc)2, H2O/THF 2. NaBH4 O 2 O 16 O 3 O 8 O 4Consider the reaction scheme below. Br2 FeBr3 .CI AICI3 NaOH Y warm What are the structures of X, Y, and Z? Include all possible substitution products.Arrange the following compounds in the increasing order of reactivity towards Conc.HNO3 & Conc.H2SO4 1. Benzene 2. Chlorobenzene 3. phenol 4. Toluene 5. Nitrobenzene A 1,2,3,4,5 B) 5,2,1,4,3 C) 5,1,4,2,3 D) 5,1,2,4,3