a. At equilibrium, the product mixture contains about 24% STAR material and about 75% product. Calculate Keq for this reaction. b. What is the approximate value of AGSuperseript double daggero C. Add curved arrows to the mechanism. d. Draw the energy diagram for the reaction.
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- Solution:- 3. Determine the amount, in of a (2.20 M s olution of dichloromethane needed to completely react with 15.72g cyclohexene to give 1,2-dibromocuclohexanw. Assume 12% excess is needed in order to react completely. a . How much 1,2 -dibromocyclohexane would theoretically be produced ? c. How many ML of the 2.20 M Br2 solution are required?1. Write down all the steps of the reaction of 2-Methyl-2-hexene with sulfuric acid and name the product formed. Will provide helpful ratings for correct solution.best condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1ene
- What is the strongest IMF in pure 2-octanone? I know it is a ketone and has some polarity due to this, but the carbon chain so long, I wonder if london dispersion forces are stronger?- For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structures of the minor and major products of the elimination. Picture: Cyclohexane (no double or triple bonds) with a methyl group and an alcohol group (HO 4e- on O) on C1 (bottom) reacting with H2SO4 -> "Major and Minor Products" -The H2SO4H2SO4 is abbreviated as H+H+ in the drawing module. Do not delete any pre‑drawn bonds, charges, or lone pairs. If you accidentally make a mistake, remove the last change by using the undo button on the lower left or revert the drawing palette to the original state by selecting the More menu, then select Reset Drawing. Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate for the elimination. (Picture 1) -Step 3: This tertiary carbocation intermediate readily undergoes…What is the dominant product of the complete hydration (2 moles) of 1-butyne (catalyst H,S04)? () butaneC 2-buteneO 1,2-butanediol0 2.2-butanediol) 1,1-butanediol
- Assuming a 56.8% yield, how kany ml of alkene is required to produce 22.5 mL of 2,3-dimethyl-2-butanol? MW of alkene: 84.16, d: 0.653 MW of 2,3-dimethy-2-butanol: 102.17, d:0.823help me please Please fill in the reagents,intermediates, and/or products of the following reactions. all the reactions shall be covered in Chapter 12-15 from Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise.Table 6.4. Oxidation: Reaction with Baeyer’s reagent (cold, dilute, neutral, aqueous KMnO4) Write (+) if the reaction is positive, (-) if negative. SAMPLE OBSERVATIONS +/- cyclohexane cyclohexene benzene toluene acetylene Enumerate the classes of hydrocarbons that are oxidizable by Baeyer’s reagent. ________________________________________________________________________ ________________________________________________________________________ What is the structural feature of these classes of hydrocarbons? ________________________________________________________________________ ________________________________________________________________________
- Draw an approximate energy diagram withannotations for the rotamers of 1,2-dibromoethanefrom 0-180°. Give the Newman projections andnames of the most important rotamers.How many mono-chlorination products are possible for 3-methylpentane? Draw them out.For 20.7 the solutions for part c and d dont seem right. Shouldn't reacting with 1 eq of H2 just take away the C=C bond and not the C=O bond. (H2 reduces C=C selectively to form a ketone according to page 738. Also the both the C=C and C=O bond should be reduced if excess H2 is used