Laboratory 11, Equilibrium Control of a Reaction Name Chemical Equilibrlum: equilibrium is when the rates of the forward and reverse reactions are equal. Therefore, the concentration of all reactants and products remain constant. This is not to say that the reaction has ceased. It is a dynamic situation at chemical equilibrium with the rate of disappearance of reactants the same...
(8 pts) For each reaction, predict what mechanism will account for the major product(s) formed and write (SN1, SN2, E1, E2 or N.R.) in the boxes provided. Explanations or drawings are NOT required. 4. а. Н-о Br heat b. OTs NaOEt НOE с. NaCl OTs DMSO d. CI CHон
13. Draw the expected major product predict the reagent for the reaction (2.5 pts for each ") 30 pts HBr ROOR --BOK/BOH enantiomer 1. 1 eq HCI 2. 1 eq HBO 1. NaNH2 3. NaNH2 HC=CH 1) Hg(OAC), HOCH,CH,CH: 2) NaBH
2P (a) Draw/predict the major elimination product(s) of the following proposed reaction. Be sure to indicate correct stereochemistry when appropriate in the product. (b) Provide a mechanism that describes the formation of your drawn product. Show how (Newman Projection) any stereochemistry within the mechanism/product results. CHз Br NAOCH3 "CH-CHз
Predict cell potential under nonstandard conditions. What is the calculated value of the cell potential at 298K for an electrochemical cell with the reaction shown below, when the [Hg2+ ]= 1.13 M and the [ Cr3+ ] = 9.02x10-4 M? 3 Hg2+ (aq) + 2 Cr (5) —— 3 Hg (1) + 2 Cr3+ (aq) Cell Potential: V
Predict whether each of the following salts is acidic, basic, or neutral. Following salts is acidic, basic, or neutral. For salts that form acidic or basic solutions, write an equation for the reaction. (a) ammonium bromide hoom 300.0 SISO NHybr 5 0.0 f or Jacocxlorcado.o (b) potassium nitrite KNO2 (c) magnesium nitrate Mg (NO2)2
O ? 1) PhMgBr 2) H,о" Incorrect. N. [H2SO4] ? - H20 Edit Incorrect. ? H RCO3H (b) X Н,С- "он Edit CH3 Predict the major product of each reaction below: ? 1) EtMgBr 2) H2O Edit SHOW HINT ? H 1) PhMgBr 2) H20 I
1. Predict the product(s) (or no reaction) and reagent(s). (17 pts) KI DCM ЕТОН heat H2O heat DBU DCM Testos e sot KNE DMF KOME DMF KOET HMPA LDA THF NaO'Bu toluene EtOH heat NaOH DMSO NaCN reagent(s); OH reagents) reagents):
6. Predict which of the following two isomers (cis- or trans-) will undergo an E2 elimination under the treatment with EtoNa in EtOH more rapidly. A) For the explanation of the reaction rate, draw chair conformations for each isomer, determine which conformation is more stable . B) Draw the major product and the mechanism of the reactions. CI cis-isomer trans-isomer
Be sure to answer all parts. Predict the product and draw a stepwise mechanism for the following reaction: oints Part 1 out of 4 eBook Print References HBr OH Report problen draw structure... Hint Organic Final Product Solution 3 attempts left Check my work Next part Guided Solution