Draw the major organic product(s) of the following reaction.DMSOCINaSCH3• You do not have to consider stereochemistry.• If no reaction occurs, draw the organic starting material.• When SN1 & E1 pathways compete, show both the substitution and the elimination products.• Separate multiple products using the + sign from the drop-down menu.• Do not include counter-ions, e.g., Na*, I*, in your answer.Θ√n [F Draw a structural formula for the substitution product of the reaction shown below.Br+Na OCH 3CH3OH• Use the wedge/hash bond tools to indicate stereochemistry where it exists.• If more than one stereoisomer of product is formed, draw both.⚫ Separate multiple products using the + sign from the drop-down menu.⚫ Products that are initially formed as ions should be drawn in their neutral forms.་+n

1) The first reaction is an E2 elimination wherein sodium methoxide is a strong base to form the E…

Answered: Draw the major organic product(s) of…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter5: Stereochemistry At Tetrahedral Centers

Section5.SE: Something Extra

Problem 75AP

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draw the two possible carbocations that can form when this alkene reacts with a strong acid (such as HBr or H3O+). of the two structures you drew, circle the more stable carbocation
The addition reaction of an acid (HBr) to an alkene (CH3CH=CH2) follows Markovnikov's rule and involves: A) initial attack by Br– B) initial attack by Br• C) isomerization of CH3CH2CH2Br D) formation of a primary carbocation. E) formation of a secondary carbonation. (F) Formation of allyl carbocation
Draw the products of the following reactions. If the products can exist as stereoisomers, show which stereoisomers are formed.a. cis-2-pentene + HClb. trans-2-pentene + HClc. 1-ethylcyclohexene + H2O + H2SO4d. 2,3-dimethyl-3-hexene + H2, Pd/Ce. 1,2-dimethylcyclohexene + HCl f. 1,2-dideuteriocyclohexene + H2, Pd/Cg. 3,3-dimethyl-1-pentene + Br2/CH2Cl2h. 1E2@3,4@dimethyl@3@heptene + H2, Pd/Ci. 1Z2@3,4@dimethyl@3@heptene + H2, Pd/Cj. 1@chloro@2@ethylcyclohexene + H2, Pd/C
C6H5CO2CH2C6H5 can be synthesized by an SN2 reaction. Draw the structures of the alkyl chloride and nucleophile that will give this compound in highest yield. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include all valence lone pairs in your answer. Separate multiple reactants using the + sign from the drop-down menu. When a metal counterion is needed, use Na+, but draw it in its own sketcher.
What are the reagents used to convert 2-butyne to C4H8? What are the products when that C4H8 is mixed with OsO4, and H2O (the formula will be C4H10O2 racemic)? What is the product when C4H8 is mixed with RCO3H, and H2O (the formula will be C4H10O2 meso)?
Draw the products of the following reactions. If the products can exist as stereoisomers, show which stereoisomers are formed. a. cis-2-pentene + HCl b. trans-2-pentene + HCl c. 1-ethylcyclohexene + H2O + H2SO4 d. 2,3-dimethyl-3-hexene + H2, Pd/C e. 1,2-dimethylcyclohexene + HCl f. 1,2-dideuteriocyclohexene + H2, Pd/C g. 3,3-dimethyl-1-pentene + Br2/CH2Cl2 h. (E)-3,4@dimethyl-3-heptene + H2, Pd/C i. (Z)-3,4-dimethyl-3-heptene + H2, Pd/C j. 1-chloro-2-ethylcyclohexene + H2 , Pd/C
Free radical halogenation is used to replace one or more hydrogens on an alkane with one or more halogens (either chlorine or bromine). It is a substitution reaction. A student performs a free radical bromination on 3-methyl-pentane (5.88 g) to create the desired product of 3-bromo-3-methyl-pentane. The product mix, which hopefully contains almost all 3-bromo-3-methyl-pentane, is cleaned up by passing it through a gas chromoatograph, which separates out the 3-bromo-3-methyl-pentane from any undesired products made during the reaction (undesired products are created frequently in free radical halogenation). The initial product mix weighed 9.45 g; the purified 3-bromo-3-methyl-pentane weighed 7.21 g. What is the student's percent recovery?
Consider the compound 3(S),5,5-trimethyl cyclohexane. Upon reduction with H2 on a 1% Pt/C catalyst, draw the equation for this reaction, find out the absolute configuration of the product and explain why the absolute configuration is completely inverted in this reaction
Fill in the missing information (reactants, products, or reagents) in the following transformations. If more than one product is possible, draw structures for all products and indicate the major product. If stereoisomers are possible, draw all isomers, and indicate the major stereoisomers.
What about the second step in the electrophilic addition of HCl to an alkene-the reaction of chloride ion with the carbocation intermediate? Is this step exergonic or endergonic? Does the transition state for this second step resemble the reactant (carbocation) or the product (alkyl chloride)? Make a rough diagram of what the transition state may look like?
How many different alkenes can be formed from the haloalkane in Figure 20? Take stereoisomerism into account. * 1 2 3 4 This haloalkane will not form an elimination product.
Please draw an alkane that has at least one primary, one secondary, and one tertiary carbon. Then take molecule and react it with F^2 (Identify all mono halogenated products for each reaction)

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