Draw the two major products of this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. ⑤ 1. BH 3-THF 2.H2O2, NaOH, H2O
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- Draw two major products of this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.Name the alkene below.Use only E/Z designators to indicate stereochemistry.Can someone please explain the logic of 2 vs 3 for stereochemistry? They are both C-C so I don't understand how to rank 2 vs 3. Thank you!
- The 1,2‑dibromide is synthesized from an alkene starting material. Draw the alkene starting material. Clearly, show stereochemistry of the alkene.a.Draw three-dimensional representations for all stereoisomers of 2chloro-3-methylpentane, and label pairs of enantiomers. b. Considering dehydrohalogenation across only C2 and C3, draw the E2 product that results from each of these alkyl halides. How many different products have you drawn? c. How are these products related to each other?Consider a reaction where cis-but-2-ene is treated with sO followed by NaHSO/H, O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- A hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.Which carbocation is more stable? CH3CH2+ or H2C=CH+||| IV Identify the least stable carbocation. A) I B) II C) III D) IV
- Draw the products of this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.i. Fill in the missing starting materials, products, or reagents as necessary. ii. Label each transformation as SN1, SN2, or acid/base. iii. Indicate if the product is racemic or a single enantiomerDraw the product of an SN2 reaction shown below. Use the dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.