Identify the MAJOR product formed in this sequence of reactions. Note: enantiomers, when formed, are omitted. Bonus: which of these products are chiral? Br 1) t-BuOK, t-BuOH 2) m-CPBA m-CPBA .OH A B C D E
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- Draw the major organic product that results in the following reaction. Include stereochemistry at the chiral center. M OH 120 1. TsCl, Pyr 2. NaCN4. Draw the structure of product, substrate or condition in the following reactions (should clearly show the stereochemistry) a) HBr (2 equiv) b) 1) NaNH2 2) Ме 1) OsO4 2) NaHSO3 c) t-BUOK t-BUOH Hint: this is the only product formedThe following chiral compound undergoes a stereospecific E2 reaction, where only one stereoisomer is produced as product. What is the product of the reaction?
- What product(s) is(are) formed in the following reaction Br/CH-Clz Br plus enantiomer H3C Et Br Br H and H3C Br H3C Et Et Br он ...Et plus enantiomer H3C BrIs fluoxetine chiral? If so, which of the possible stereoisomers are formed in this synthesis?Draw the stereoisomeric products for the following reaction. Please draw all four bonds, including those to hydrogen, at all chiral centers.
- Please be a hundred percent sure your answer is correctFor the following reaction, decide whether a solution of the products would be optically active or not and why. You will need to know the product of this reaction in order to solve this problem. To preview the image click here Br CH3 Na: CEN: acetone O Not optically active, achiral product is formed O Not optically active, racemic mixture is formed O Not optically active, a meso compound is formed O Optically active, a single enantiomer is formedWhich carbocation is the most stabilized? Me Me CO₂Me MeO A B C D Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a A b B CC OMe Me Me OMe Me Me MeO. OMe E Me Me
- Is dinocap chiral? If so, which of the possible stereoisomers are formed in this synthesis?Use mechanism arrows to show the mechanism indicated for each reaction. Draw all possible regiochemical and stereochemical products and indicate if the reaction solution is optically active or not. OTS Ph NaNH, SN2 CH₂OH SN1 Is the reaction solution optically active: yes or no?. Is the reaction solution optically active: yes or no?Draw the products of these reactions clearly showing stereochemistry in each case if necessary. If the product is formed as a racemic mixture, clearly draw one stereoisomer with dash/wedge bonds and write “+en”. Circle whether each reaction occurs by an SN1 or SN2 pathway.