3.10 (a) The equilibrium for this acid-base reaction will be on the left hand side .
The detail explaination is shown below.
which side is more stable and why? 3.10 Determine the position of equilibrium for each acid-base...
7. Which statement is true about the acid/base equilibrium reaction? ASH OH (A) The right side is favored because the base on the right side is the stronger of the two bases. (B) The right side is favored because the base on the right side is more stable. (C) The left side is favored because the base on the left side is weaker. (D) The right side is favored because we always draw reactions such that the right side is...
#1 Use a table of bond disassociation energies to determine which side of this equilibrium is favored (ie, which direction would the reaction go to form the more stable product?) ~ o . HOW Br + H-OH = nom . Her ~ OH + H-Br
Q 33 - (2 pts) Predict the position of equilibrium for the following acid-base reaction. + A) reactants side (Keq <1); B) products side (Keq >1); C) reactants and products are at the equilibrium (Keq =1);
please explain 2. (A) Draw the products of the acid/base reaction, (B) determine the position of the equilibrium, (C) use curved arrows to show the mechanism of the reaction and (D) briefly answer "Would water be suitable to protonate the carboxylic acid?". (8 pts) H-O + F3C H
Q 10- For the following acid-base reaction, predict which side the equilibrium is favored (circle or draw an arrow pointing the favored side). Calculate the Keg from the pKa given. PK, -30 Kea pk, 10
1. For each reaction below Classify each acid, base, conjugate acid, and conjugate base as a strong acid, weak acid, strong base, or a weak base. Calculate the value of the equilibrium constant II. I. Determine if these reactions need to be treated as an equilibrium (needing an ICE table) or a stoichiometry problem (assuming the reaction goes essentially to completion) a. F-(aq) H2O() HF(aq) + H3O*(aq) + H2O(1) NH3(aq) + b. NH4 (aq) OH (aq) + H3O*(aq) NH3(aq) +...
1. Which position is more stable for the methyl group in methylcyclohexane: an equatorial position or an axial position? Explain your answer. 2. Draw the Fisher projections for the pair of enantiomers of lactic acid, CH3–CH(OH)–COOH. 3. For 2,3-dibromobutane: a. How many stereoisomers are possible for the compound? Br Br | | CH3–CH–CH–CH3 b. Draw Fisher projections for each stereoisomer, label enantiomers. Label any meso 4. Determine the relationship between the following pairs of...
Label each species in the following equation as either a Bronsted acid or base. Determine the position of equilibrium by dragging in the appropriate arrows. Use the data below to estimate the K_eq of the forward reaction. k_eq =
3.46 For each reaction below, draw a mechanism (curved arrows) and then predict which side of the reaction is favored under equilibrium conditions: ОН HO + ol (a) HOH (b) ~ SH + + 2 OH SO H.S urs aw (c) SH = 1
2. For the following acid-base equilibrium H-BH + Acid Base Conjugate Base Conjugate Acid (a) Draw a curved arrow mechanism above to show the transfer of a proton from the starting acid "acetylene" to the starting base "n-butyllithium"(two curved arrows are necessary). (b) Draw the conjugate base of acetylene and the conjugate acid of n-butyllithium, indicating all counter ions and formal charges in the rectangles provided above. (c) Which side. Left or Right, of this equilibrium is favored thermodynamically? What...