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- Compound X, shown below, spontaneously reacts via an intramolecular SN2 to produce intermediate Y, known as an "aziridinium" ion. In the presence of water, intermediate Y reacts further to form product Z. What is the identity of product Z. OH (A) + En Br O (B) aziridinium ion Y OH (C) H₂O + En Z HOFor each one of the following reactions, show step by step mechanism of the reactions and indicate the stereochemistry of the products and their relationshipHS 18.5 Give the intermediate formed in the first step and suggest reagents for the second step. 1) NaOH 2) Br
- Grignard reagents react with a variety of different compounds. What are the expected products from the following reaction?2,4-D is a synthetic auxin (a plant hormone) used in the control of broadleaf weeds, and one of the most widely used herbicides in the world. It is produced commercially by the following reaction: chloroacetic acid + dichlorophenol → hydrochloric acid + 2,4-D C2H3ClO2 + C6H4Cl2O → HCl + C8H6Cl2O3 How much chloroacetic acid does it take to manufacture 5.18 grams of 2,4-D?East Indian sandalwood oil contains a hydrocarbon given the name santene (C9H14). Ozonolysis of santene gives the compound shown. What is the structure of santene?
- How many potential E2 elimination products can form from the addition of NaOH to the following: (free hint: trans-decalin cannot undergo a ring flip) → 1/2/3/no products H Br "H. H, BrIdentify the major product in each of the following reactions:What product(s) would you expect from reaction of (S)-3-chloro-3- methylheptane with acetic acid? Show the stereochemistry of both reactant and product.
- Birch Reduction of toluene leads to a product, X with the molecular formula C7H10. After ozonolysis of X, the two compounds, 3-oxobutanal and malonaldehyde are formed. what is the structure of xQuestion 7Select the kinetic and thermodynamic products of the reaction shown. HBr Part 1 Select the kinetic product: Choose one: