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- 3. Draw mechanism and predict product niwollo) ardnot abog ojs ed 1bo19 (q) 1. NaOH H. 2.14) what type of chemicall reaction in the follasing example? is illustrated so Ca)キ cambination reaction decomposi tion reaction Single-veplacement reactian noutralizathon reactionn double -ement reactian replaceFor the reaction below, draw a step-by-Step mechanism (ar rOus men drawa reaction Coordinate diagram as well as mě Struckare of she ransHlon state m for the reacon mechanism for the first Step in the mechanism consist ent with me Hammond Postulate : Но -Br CH gCH2OH + HBr
- The clecona position of nitramide. ) Solutionat 25°C in.ayueous. NH2NO2 la)- has the Follacing reahonship between rate and concentrahionwhere the bracket anund thse formula indicates concentration and K is a Constant caled the rate constant. hate K [NH2NO2] IF the value of Kis l6.49x10s-1 rate of the reaction when MH,NO=0.3016M? -5 what is the Ms-please and the produet of the Follobing reaction provide the mechanism NaCN ->istory Bookmarks Profiles eriment 11B Part X = ALEKS Substrate A CI O SUBSTITUTION REACTIONS Predicting the effect of carbocation stability on the rate of... O Tab aleks.com/alekscgi/x/lsl.exe/1o_u-IgNslkr7j8P3jH-liGBdp5ulp5VqUnMDyPOVaX6q0CRPLZSQ5Ne1rFYH1k1 Window Help Br CI For each pair of substrates below, choose the one that will react faster in a substitution reaction, assuming that: 1. the rate of substitution doesn't depend on nucleophile concentration and 2. the products are a roughly 50/50 mixture of enantiomers. X Substrate B St. ..... B O ALEKS - Tiffany Te-L-Peng - L X Faster Rate (Choose one) (Choose one) + (Choose one) ▼ X
- 6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HOWhich of tne 40llowing compounds could be a Micnael reaction ccircle all po 35ible anouwers)? prodluct of theOMe O OMe mechanism requires PdCl₂ (cat) A CUCI, O₂ H₂O
- 0 a +H=BC: Where are the curved arrow poshing mechanism as well as the non-bonding electrons. What are the initiation and progation Steps? •What are the two termination Steps for the reaction. B. с A. В. C. D. Brz HV - + • Br: → H-Br: + → + • Br: H-Br: + H + • Br: → H-BC: + •Where are the curved arrows pushing the reaction with bromine atom? What are the radical product including the resonance contributors • Rane the reaction in order of increasing rate. what is the explanation that includes the term Hammond Poštutate? H2 PJ/C HBI Br: 1.BH 3. THE 2. NaOHV/H₂O₂ Bcz (2) hu x 1. What are the major organic productes) of the reaction. Include all Stereochemistry and identify any meso compounds. E.. все hu 2. Would the solution of the products be optically active of not active. what would be the Ceason for the choice?3. Draw the complete reaction mechanism in each step for the formation of compound C and D. i) ) PdCl (M CN), 1) -CH(CO,Et); Ph Ph. Ph (EtO,C)HC, N O li) co H- 60 - 95% R 97% de iv) Me,SnR co,Me ÓTMS Pd(OAc)2 CH,CN CO2Et 55%Predict the products of each reaction. If the product has stereochemistry, draw the products using dash wedge notation. Draw all stereoisomers formed and indicate if the product is achiral or chiral. Draw a mechanism for each reaction clearly showing how the product stereochemistry is produced. You are not required to draw the final step(s) in the mechanism for reactions involving organometallic intermediates.