Print Last Name, First Name InitialStatifically more chances to abstract one of these 6H11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 44th total• 6H total래• 4H total21 totalZH2HStatisticalH < 3° C-H weakest-productabstraction herebundleads to thermo favoreda) (6pts) How many unique mono-chlorinated products can be formed and what are thestructures for the thermodynamically and statistically favored products?Product6Number of UniqueMono-Chlorinated ProductsThermodynamicallyFavored ProductStatisticallyFavored Productb) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for theformation of the thermodynamically favored product. Only draw the p-1 step. You donot need to include lone pairs of electrons. No enthalpy calculation necessaryHH-ClWaterfox

Part (a): Number of Unique Mono-Chlorinated ProductsIdentify unique hydrogen atoms: Based on the…

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Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry

Section4.SE: Something Extra

Problem 51AP

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Last Name, Firs Statifically more chances to abstract one of these 6H 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 • 6H total $ 4th total 21 total 4H total ZH 2H Statistical H < 3°C-H werkst - product bund abstraction here leads to the mo favored a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? Proclict 6 Number of Unique Mono-Chlorinated Products f Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary 'H H-Cl Waterfox
Chances Ad ~stract one 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 • 6H total $4th total Statistical pro 21 total 2 H A 2H 래 • 4H totul < 3°C-H werkest bund - abstraction he leads to then mo fac a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? рос 6 -વા J Number of Unique Mono-Chlorinated Products Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary H H-Cl
Q2- Which one of the following reaction is unreasonabl? A) NaOH(aq)+HCl(aq)-NaCla+H₂O B) H2(g)+1/202)→ H₂Op AHneutralization=-851.5kJ/mol =-283.5kJ/mol AHormation C) CH3COOH + H₂O-CH:COO(g) + H AHassociation = +213.5kJ/mol D) Mg(+2HCl → MgCha) + H₂ - AHformation =+315.5kJ/mol Q3- If A 25.0 mL of diluted bleach solution has required 30 mL of 0.30 M Na S,O; to reach the endpoint of the titration. Calculate the mass percent of NaCIO in the original sample (Molar mass NaCIO = 74.5 g/mol). Assume the density of bleach solution is 1.084g/mL and the dilution factor is 10. B) 9.96% C) 0.996% D) 12.4% A) 19.92% and the colo
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Predict the product for the following reaction. H₂C A I and II HH3C xoxoxox B D IV E cis-1-bromo-3-methylcyclohexane ||| SH H₂C NASH III acetone Br H3C ||||SH IV H
C OWLV2 | Online teaching and learning resource [Review Topics] [References] Use the References to access important values if needed for this question. Draw the structural formula of the product that would form when 1,3,4-trimethylcyclopentene undergoes catalytic hydrogenation. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. C opy aste ChemDoodle M) Submit Answer Retry Entire Group 4 more group attempts remaining Previous Next Email Instructor Save and Exit
63°F Partly sunny Predict the product of the following reaction. H₂O Heat Draw the molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. NN ● [1] A осо A H₂CrO4 H₂SO4 Submit Request Answer 1 H 12D EXP. CONT. L CONT. ?** Im Marvin JS by ChemAxon Search PRE H C N O S CI Br - P F Ty I -- O
Organic Chemistry Мaxwell presented by Macmillan Learning For the dehydrohalogenation (E2) reaction shown, draw the major organic product. Select Draw Rings More Erase H CH;CH2OK CH3CH2OH heat Br
urgent pls help answer both questions
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[17] H What is corect name of following? CH2CH3 HO CH3 Br 2R,35-2-brome. (2R,3S) 2-bromo-3-hydroxy pentane (2R,3R) 2-bromo-3-hydroxy pentane ((25,3S) 2-bromo-3-hydroxy pentane (01 اورا (S) 2-bromo-3-hydroxy pentane (2S,3R) 2-bromo-3-hydroxy pentane 3hr [18] Which of following compound will undergo solvolysis with methanol to yield the two shown? H3C OCH 3 CH3 CH3 OCH3 (a) (15,3S)-1-bromo-1,3-dimethyl-cyclohexane (b) (1R,3R)-1-bromo-1,3-dimethyl-cyclohexane (c) (15,3R)-1-bromo-1,3-dimethyl-cyclohexane (4) (1R)-1-bromo-1,3-dimethyl-cyclohexane (e) (15)-1-bromo-1,3-dimethyl-cyclohexane
Rank the following alkenes in order of increasing reactivity to hydrogenation. A) | < || < III B) | < III < II C) || < ||| < | D) ||| < || < | E) III < | < || Question 15 of 41 Tap here or pull up for additional resources Submit

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