Assume you have carried out a radical chlorination reaction of (R)-2-chloropentane and have isolated (in low yield) 2,4-dichloropentane. Which pair of products correctly depicts the stereoisomers of the product CI H,
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- Assume you have carried out a radical chlorination reaction of (R)-2-chloropentane and have isolated (in low yield) 2,4-dichloropentane. Which pair of products correctly depicts the stereoisomers of the product? CI H, H, R '"A student adds NBS to a solution of 1-methylcyclohexene and irradiates the mixture with a sunlamp until all the NBS has reacted. After a careful distillation, the product mixture contains two major products of formula C7H11Br. (a)Rank these three intermediates from most stable to least stable.Complete the following reaction by drawing a structural formula for the product. CH,CH, (1) NABH4 ? (2) H30* • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms.
- Draw the structural formula of the product of the reaction shown below. + H₂O AAVIL H₂SO4 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. Sn [F Ⓡ ChemDoodleFor the molecule given, prioritize each substituent on the stereogenic carbon, and assign absolute stereochemistry. Part: 0 / 2 Part 1 of 2 Cl Assign priority to each substituent. -CH,O- - CH3 - CH₂0¹8- - C1 (Choose one) ▼ (Choose one) (Choose one) ▼ (Choose one) ▼ XThe 2 +2 cycloaddition of two molecules of (2E) -2- butenedinitrile leads to what product? Describe this process using a reaction scheme and curved arrows, show the product including the stereochemistry of the product.
- Draw a structural formula for the major organic product of the following reaction: CH2CI2 Br2 CH3CH=CHCH2CH(CH3)2 + Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If enantiomers are formed, just draw one. opy aste - [F ChemDoodle1. In the lecture on the reactions of alkenes, we studied the reaction of alkenes with N- Bromosuccinimide (NBS), which went through a mechanism involving an allylic radical (the radical is a carbon attached to a carbon involved in a л bond). What if there were a conjugated system? Draw, using curved arrows, the three resonance forms of cyclohexadienyl radical:When the alkene A was treated first with Hg(OAc)2 in MeOH and second with NaBH4 the product was the ether B. Using curved arrows please give the mechanism for the first step of (Hg(OAc)2 in MeOH) this reaction, including any regioselectivity or stereoselectivity. H3C 1. Hg(OAc)2, MeOH H3C O-CH3 =CH2 ✓ -CH3 H3C 2. NaBH H3C A B
- Draw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H₂O. Explain how these reactions illustrate that syn dihydroxylation is stereospecific. Part 1 out of 5 How many unique stereoisomers exist for the product of the reaction involving cis-but-2-ene?Name (including E/Z stereochemistry) the five alkenes that can produce 3-bromo-3-methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.Compounds X and Y are both C5H11CI products formed in the radical chlorination of pentane. Base-promoted E2 elimination of X and Y gives, in each case, a single C5H10 alkene (ignoring double bond stereochemistry). Both X and Y react in SN2 fashion with sodium iodide in acetone; Y reacts faster than X. What is the structure of Y? • Do not use stereobonds in your answer. • In cases where there is more than one possible structure for each molecule, just give one for each. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. ChemDoodle (Previous Next