Q: Question 21
A: The given data shows the concentration of a substance [A] at different times during a reaction,…
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A: Question 23 The reaction is exothermic.In the diagram, the potential energy of the products (Z) is…
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Q: Question 38
A: Question 38:
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Q: Consider the equilibrium: H2(g) + Br2(g) ⇌ 2 HBr(g) Kp = 9.89 To a 2.0 L flask are added…
A: Step 1: Before answering this question, the initial concentration of H2 and HBr must be calculated…
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Q: A sample of gas contains 1.97 moles at 37.8 °C in a volume of 3.61 L. At what pressure is this gas,…
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Q: Question 10
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Q: 17
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Q: PbO2 + I2 = Pb^2+ + IO3^-
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- Draw the structure of all products of the mechanism below. H H Yes- :Br: Continue H Click and drag to start drawing a structure. X Save For Later [H + 鸟四面 D Är Submit Assignment> Predict the major product of the following process. 1) Me2NH, [H*], (-H₂O) 2) O r Cuban Tree Fro 3) H30* ?What will be the major product of the following reaction and what is the likely mechanism for its formation? (CH;);COK Br racemic OCCCH3)3 OCCH3)3 ÓCCCH3)3 A B C D E
- Draw the major organic product of the reaction shown below. O Ca OH **** + HBr • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. - ] Jn [1 ChemDoodleⓇ 5bFor the following reaction, draw a reasonable mechanism showing stereochemistry XS H-CI xs Br-Br H OH2 H.g-H 1) 2) H2O2, OH-Q2
- Please give the structure of major product with proper mechanism.Addition of hydrochloride acid to 1-isopropenyl-1-methylcyclopentane generates 1-chloro-1,2,2 trimethylcyclohexane. Draw the complete mechanism, including intermediates, to illustrate electron flow in the reaction.Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions NOC XT :: [MgX]* H3C-C-0-CH3 CH₂CH₂CH3 :0: || H3C-C-CH₂CH₂CH3 + HạC—O: [MgX]* A ketone X
- Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions X→UU :0: :O: || CH3-C-CH₂-C-OEt :OEt :O: || :0: || CH3-C—CH—C—0—OEt + EtO: Hdraw the mechanism for the non-concerted stepwise process of this reaction (with curly arrows) and draw mechanism for the concerted cycloaddition please provide the mechanism for both reactions with curly arrows. (E)-V,1-diphenylmethanimine G InCl,(cat), CH,CN rt, 1 h (3aR,45,9bS)-4-phenyl-3a,4,5,9b-1 tetrahydro-3H- cyclopenta[e]quinolineplease write out answers and explanations to make it easy to understand
