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- 101. The major product formed in the following reaction sequence GHI Br (a) (b) (i) Br₂, H₂O (ii) H2SO4,A 'Br Br (c) All Bowl Chemistry Br (d)7. Ozonolysis of compound A yields pentane-2,4-dione. What is the structure of compound A? a OH OH H Compound A C10H16 H₂SO4 1.03 2) (CH3)2S Draw the structures of the two possible cyclization products. pentane-2,4-dione6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HO
- For the reaction below, which one of the following possible products is most likely to form? (CH3)3CONA THE Br https://ibb.co/4TPJ2LH e https://ibb.co/2s1mWP9 2 https://ibb.co/fHsfhft a https://ibb.co/y0Cn8jY OcICHals https://ibb.co/CtzHTbx 2 https://ibb.co/ZghTKD6 e(dehydrobromination) A chemist carried out an elimination reaction of 1,1-dimethyl-2- bromocyclopentane. The chemist expected the reaction to yield alkene Z as product. However, alkene Z DID NOT form. Instead, three alkenes were produced: one alkene was the major product, the other two alkenes was the minor products. What was the major alkene product that formed? Br Select one: A. I B. II C. IV D. III alcohol HEAT || Z = + (HBr) IVapp.101edu.co Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. esc F1 CH3CH2CH2OH H2SO4 (cat), heat ☀ F2 80 F3 OH a F4 W Q F5 Atoms and P Draw or ta MacBook A C F6
- Which reaction would yield cyclopentanol? سیدگی (A) (B) -d (C) (D) 1. LiAlH4 2. H+ 1. NaBH4 2. H+ 1. BHg:THF 2. H2O2, NaOH OSO4The accepted mechanism for a rearrangement reaction is shown below. "Q Ph (1) (ii) Ph Ph HO™ fast Ph Ph HO O™ slow Ph aufae .Ar² LOH HO™ fast Draw a curly arrow mechanism for this transformation. Sketch an energy profile for this reaction, showing approximate relative energies for the reactants, intermediates, transition states, and products. HQ Ph (iii) When DO™ was used as the reagent, the rate of product formation was same as for HO™. Explain why this result shows that the third step is fast and cannot be rate-determining. Ph (iv) Write the predicted rate equation for this mechanism, and show how it was derived. (v) The starting diketone may have two different aryl groups, as shown below. Propose a ¹³℃ labelling experiment that would allow you to distinguish which of the two aryl groups had migrated in this situation. OH AR²0- Ar¹ C CChemistry 4. Draw the correct product (may be multiple competing products) and label each of them as the product of E1, E2, SN1, or SN2. Br oner Br- OTS KCN DMSO NaOH H₂O, heat H₂O CH,CH,ONa CH₂CH₂OH NaSH DMSO KOH DMSO NINH, NH₂ NH₂ please explain
- 7. Give the final product 1) 480+ 2) H2Cr2O7 3) RCO₂H 4) excess LAH 5) H₂O он b) HO- он <) HO- но онTrimethyllead hydride, (CH3)3PbH, can react with methyl bromide (CH3Br) in a homolytic dissociation reaction. What will the lead-containing product be? (CH3)2Pb PbBr2 (CH3)3PbBr Pb metal2) Predict the Product(s). Predict the major product(s) for the following reactions. но. OH H₂50, (cat.), heat