For each of the following elementary steps, draw a possible transition state (activated complex).
Elementary Step) S-O + O=O → O=S=O + O
Elementary Step) N + N=O → N2 + O
Elementary Step) 2 NO + Br2 → 2 NOBr
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For each of the following elementary steps, draw a possible transition state (activated complex). Elementary Step)...
Predict the major product of the following reaction, and draw complete mechanisms for the initiation and propagation steps. Propose 2 termination steps. Label each elementary step. Br2 hv Initiation: Propagation: Predict the major product of the following reaction, and draw complete mechanisms for the initiation and propagation steps. Propose 2 termination steps. Label each elementary step. Br2 hv Initiation: Propagation:
a) Consider sider this two-step reaction. Draw the structure for the transition state in each step of the mechanism. arly show any partially broken or partially formed bonds. Include only the hydrogens shown. (0.6 pts) Step 1 Step 2 (b) How many partially formed or partially broken bonds are found in the transition state structure for step 1? # of partially formed bonds (step 1) = ; # of partially broken bonds (step 1) = Will AH® for this reaction...
5. Draw a complete mechanism for the following reactions. Show all elementary steps and intermediates (if S2. sketch what the transition state looks like), show all lone pairs, formal charges, appropriate arrows and stereochemistry. Reaction of cyclohexanol with HCl to make chlorocyclohexane in solvent ethanol. b) Reaction of ethanol with HBr to make bromoethane.
Potential energy Reaction progress First, indicate on the diagram the activation energy, transition state, and the change of enthalpy for every step of this step-wise process, as well as the change in enthalpy for the overall reaction. Then, answer the following questions: (i) How many elementary steps are there in the mechanism of this reaction? (ii) Which of these steps is the rate-determining step? (iii) How many of the individual steps are exothermic? (iv) Is the overall reaction endothermic or...
22) (5) Draw an elementary step by elementary step mechanism for the following transformation. + HCI CI
1. [Mn(H2O)6]2* Draw the possible stereoisomers. Give the oxidation state of the metal. Identify the donor atoms. Draw the structure of the transition metal complex ion. Show the charge on the complex. Determine if its paramagnetic. State whether the complex is high-spin or low-spin. Draw the ground state arrangement of the d-electrons. Calculate the LFSE (in units of A or AT) for each complex.
Use the generic elementary steps shown to below to answer the following questions. A + BC + D Elementary Step 1 (slow) A + DC + E Elementary Step 2 (fast) a. Based on the provided elementary steps, but is the net reaction? Select] [Select] 2A+B+D -> 2C+D+E 2A+B --> 2C+E termediates in this reaction? [Select] 2A +B+D -> 2C+E 2A + B --> 2C+D+E C. If step 115 the slow step, what should be the rate law for this...
Please do this step by step!! PROBLEM 4.16 The bromination of methane proceeds through the following steps: AH® (per mole) E (per mole) Br2 h, 2 Br +192 kJ (46 kcal) 192 kJ (46 kcal) CH4 + Br − CH3 + HBr 67 kJ (16 kcal) 75 kJ (18 kcal) -CH3 + Br2 → CH BrBr: -101 kJ (-24 kcal) 4kJ (1 kcal) (a) Draw a complete reaction-energy diagram for this reaction. (b) Label the rate-limiting step. (c) Draw the...
The following diagram shows the energy of a reaction as the reaction progresses. Label each of the following in the energy diagram by matching and answer whether this reaction is endothermic or exothermic. 1 [ Choose ] product reactant endothermic exothermic enthalpy of reaction activation energy activated complex (transition state) 2 [ Choose...
Draw the curved arrow notation for each elementary step of the mechanism described below. In each step, be sure to include all relevant electron pairs, reactants, and products. NOTE: you are showing a mechanlsm. Therefore, the product from elementary step 1 is the starting materlal for 2, the product from 2 is the starting material for 3, and so on. 2. 1) proton transfer involving HCI 2) heterolysis OH 3) carbocation rearrangement 4) electrophilic addition involving benzene (CgHg) 5) electrophilic.elimination