Either the reactant (X) or the major organic product is missing from the equation below. Draw the missing compound. 0 CH2 CH₂CCH₂CCH2 CH3CCH2CCH2CH3 Pd/C + H2 (1 equivalent) • You do not have to consider stereochemistry. . In the case of a missing reactant, there may be more than one answer. If so, draw all possible reactants in separate windows. . Separate structures with + signs from the drop-down menu. + n D
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- The molecules below react in a displacement reaction. Determine the products) and assign configuration (R/S) to any stereogenic centers in the product. The Cahn-Ingold - Prelog rules can be used to assign priority to the four different groups on a stereogenic center.For each section, circle the mechanism from the two options given (SN1 or SN2) and draw the main organic product resulting from that mechanism. Indicate the stereochemistry and if two configurational isomers form, draw both.Provide the major product of the reaction sequence. If cis/trans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration.
- Draw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic no stick structure don't understand 3,4-dimethylhex-3-ene with BH3. After reaction is complete, add H2O2, –OH, and H2OHello, could someone help me with this practice problem? thx in advance (: For the major product of this reaction, draw the perspective diagram of the major products. The mechanism isn't necessary, just the products. If appropriate, add an enantiomer where required. Lastly, state the stereochemistry of the process (syn, anti or none).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 enantiomer
- In some nucleophilic substitutions under SN1 conditions, complete racemization does not occur and a small excess of one enantiomer is present. For example, treatment of optically pure 1-bromo-1-phenylpropane with water forms 1- phenylpropan-1-ol. (a) Calculate how much of each enantiomer is present using the given optical rotation data. (b) Whichproduct predominates—the product of inversion or the product of retention of conguration? (c) Suggest an explanation for this phenomenon.Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the structure of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts.?Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after workup to neutralize acid. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
- Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. You do not have to consider stereochemistry. If no reaction occurs, draw the organic starting material. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Since conformer A can undergo E2 elimination, using this conformer need help providing a mechanism for the elimination to provide the expected product 2, 3 or 4 and explain why only this product forms (see picture that shows what 2, 3 and 4 are). Thank you :)Please answer the subparts 4, 5, 6 and 7. Please mention all the mechanism and needed reagents. Thanks