Consider the following reaction. NaOCH,CH, Part: 0/2 Part 1 of 2 Draw the alkyl halide in the conformation that is required for an E2 reaction to occur. Use a wedge and dash structure for your answer. 7:0
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- Consider the following reaction. Br Part: 0/2 NaOCH,CH, Draw the alkyl halide in the conformation that is required for an E2 reaction to occur. Use a wedge and dash structure for your answer. Part 1 of 2 Click and drag to start drawing a structure х :☐ G PConsider the following reaction. NaOCH2CH Draw the alkyl halide in the conformation that is required for an E2 reaction to occur. Use a wedge and dash structure for your answer. X 8:0 G PConsider the following reaction. Part: 0 / 2 Part 1 of 2 Br NaOCH, CH Draw the alkyl halide in the conformation that is required for an E2 reaction to occur. Use a wedge and dash structure for your answer. Click and drag to start drawing a structure. ☑ :
- Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert-butyl bromide in methanol, and arrange the correct mechanism for its formation. Be sure to answer all parts.Draw the alkene structure that produced the following compounds in a ozonolysis reaction as specified. 1. O3 2. (CH3)2S You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one.Draw the bond-line (skeletal) structure of the compound with molecular formula C₂H₁3Br that gives the following alkene as the exclusive product of E2 elimination. Click and drag to start drawing a structure. C X C Ś c+
- Explain why heats of hydrogenation cannot be used to determine the relative stability of 2-methylpent-2-ene and 3-methylpent-1-ene. A, B, and C, each subjected to hydrogenation. The number of rings and π bonds refers to the reactant (A, B, or C) prior to hydrogenation.a. Draw the two chair forms for compound A, being careful to show the stereoisomergiven above. You may use shorthand R in your drawings. Indicate the MAJOR and MINORconformations b. Using curved-arrow convention and the correct chair form of Compound A, show themechanism for the formation of alkene C from Compound A. You may use B: to indicatethe base.Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor product. (a) Draw a stepwise mechanism that shows how this alkene is formed. (b) Draw other alkenes formed in this dehydration. At least one must contain a five-membered ring.
- Draw all stereoisomers formed in the reaction shown. Use wedges and dashes for tetrahedral stereogenic centers, if applicable. OH CH₂CH₂OH HClDraw the product of the reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts. 1. NaCN 2. H₂O Drawing9. Hydrates, in which two -OH groups are connected to the same carbon, are not favorable except in a few cases. One case is: a) acetaldehyde c) acetone b) formaldehyde d) chloroform 10. The Wolff-Kishner reaction, in which an aldehyde or ketone is treated with NH2NH2 and KOH, is: a) an oxidation c) an SN2 reaction b) a reduction d) a hydration 11. Which of these is most likely to dissolve in 5% NaOH? a) 1-decanol b) decanal c) decanoic acid d) 2-decanone bu itcolf Draw tbe