V Arter running various experiments, you determine that the rate law for the following reaction has a first-order dependence on the concentration of the alkyl halide, and doesn't depend on the concentration of the other reactant at all. Br + H₂O OH2 + Br Using this information, draw the correct mechanism in the space below. Explanation Check टे Add/Remove step Br Click and drag to start drawing a structure. 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Acces
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- 08:32 A ¢ READ-ONLY - This is an older file format. T.. 1 Part II Q1. Complete any three of the following reactions with mechanism. CH-CH-CH3-CH; i) KMno, Heat NABH, NaOH iii) 2 NH,-X iv) II %3D2- Write step-by-step mechanism for the following reaction: Cul R1 но .*...... ....... ........Consider the reaction below: Br H₂O heat OH to 1. The reaction mechanism for the reaction is choose your answer... 2. The nucleophile in the reaction is a choose your answer... ✓nucleophile.
- The following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with "CN. The experimental rate law for this reaction is Rate k [S-3-chloro-2-methylhexane] CH3 H;C. C. C H. CH3 CEN H2 H. The mechanism for this reaction is SN1 Draw the orgamic molecule(s) which is(are) formed in this reaction. Do not include molecules like H,O or HCl. Draw the specific configuration (R or S) at any chiral carbons within your product(s). If both configurations are formed in the product(s), draw both as separate molecules/products.a) Sketch the energy diagram for the conversion of tertiary butyl bromide to methyl t-butyl ether. Note that this is a two step reaction with the t-butyl cation as an intermediate. Assume that this is overall an exothermic reaction. Show the location of both transition states and the intermediate. The first step has the higher energy of activation and is the rate determining step. (CH3)3C-Br ------> (CH3)3C+ + Br- (CH3)3C+ + H3CO- ------> (CH3)3C-O-CH3 (b)Draw the curved arrow mechanism and the transition state when the tertiary butyl carbocation reacts with the methoxide ion to give an ether. (CH3)3C+ + H3CO- ------> (CH3)3C-O-CH37. Condensation Polymers oliya + CI + H₂N. NH₂ H₂SO4 + n + nHCI n HCI For the second reaction above, show the full mechanism for one addition of the two monomers (3 steps).
- After running various experiments, you determine that the rate law for the following reaction has a first-order dependence on the concentration of the alkyl halide, and doesn't depend on the concentration of the other reactant at all. Br + H₂O + H30* + Br Using this information, draw the correct mechanism in the space below. Br Add/Remove step X G Click and drag to start drawing a structure.3) Fill in the red box(es) with the missing reactant(s), reagent(s), product(s), solvent, and/or conditions and write a reasonable mechanism for the reaction. Not every box needs to be used and not every box necessarily corresponds to only a single species. If no reaction occurs OR no reagents exist to perform the reaction state, “NOT POSSIBLE” AND explain why. HO OH dil. H₂SO4For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be true for one or moremechanisms. The reaction rate increases when the solvent is changed from CH3OHto (CH3)2SO.
- 1. Reaction mechanism 2. Show sterochemistryPlease10. practice q 10 Compound A reacts with B in the presence of sodium hydride to give C as a major product. HO Free Energy A NH₂ + Ph ŌSO₂CF3 B NaH, THF a) Provide a detailed mechanism for the formation of C and draw it in the box above. C b) Draw the reaction coordinate diagram of that reaction. Indicate with an arrow the rate- determining step of the reaction then draw its transition state: Reaction Coordinate