I believe the rxn is an acid addition. АСФА рритон НСІ
Which element has the least electron affinity? Cl S Ne K I believe Cl has the highest affinity but I am confused about the least?...
Use Hess?s law to calculate ?G°rxn using the following information. ClO(g) + O3(g) ? Cl(g) + 2 O2(g) ?G°rxn = ? 2 O3(g)? 3 O2(g) ?G°rxn = +489.6 kJ Cl(g) + O3(g) ? ClO(g) + O2(g) ?G°rxn = -34.5 kJ
I have an proton NMR for a compound that I believe to be Salicylic Acid. It has major peaks at 11.0 ppm as well as around 10.5 ppm. Both peaks are broad singlets indicating that they should be -OH peaks. However, the typical Phenol has a peak around 5-6 ppm. Could it be possible that the aromatic ring and carbonyl group from the carboxylic acid influenced the phenol group enough to shift it that far downfield?
need help with this part benzene carbocation intermediate DOES NOT Critical Thinking Questions 1. For Rxn 1 (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1: Reaction Diagrams for Electrophilic Addition of HCI V.E. V.E. (Potential Energy) H-C1 H-C1 carbocation intermediate Reaction Progress (Rxn 2) Reaction Progress (Rxn 1) 2. Rxn 1 is slightly down-hill in terms of energy. Rxn 2 is very up-hill in terms...
I CH3 H-Cl CH3 CH3 Cl Addition of HCI to 1-isopropenyl-1-methylcyclopentane yields 1-chloro-1,2,2-trimethyleyclohexane in several steps. Propose a mechanism, using curved arrows to show the movement of electrons, for the step shown below. H3C CH3 C-CH3 CCH3 CH3 pt pt Next)
id to locus in Chem, he i symer that is a The mechanism for the addition of hydrochloric acid to 1-ethyl-1-vinylcyclopentane occurs through a ring expansion mechanism. Draw the mechanism of this reaction in ChemDraw using the ACS style template. Indicate the transition state of the ring opening step using brackets and the i symbol, dashed lines for bonds breaking and forming, indicate all partial charges with a 8. Also, indicate the "H" that is added in Markovnikov fashion to...
please draw out the acid base reaction between methyl-trans-cinnamate and sodium bicarbonate!! Krew acid base rxn with with sodium bicarbonare sodium methyl trany sodium cinnamatex Sodium bica bcnote) drops Cohio O₂ + NaHCO A-Iml methanol - small amtok trans-cinnamic acid i ml Sodium - biralbonatel arid base
Consider the addition reaction shown. 2 Cl, → product H-C=C-H Draw the product for the addition reaction. Select Rings Draw More Erase cl
Cl, ?? ??? ?? 17.0 Based on the structures of acetic acid and trichloroacetic acid, one can predict: a. b. c. d. The electronegative Cl atom makes the O-H more polar; The ionization of both are almost identical; The Cl is too far away from the O-H to make a difference; The acetic acid is more easily ionized than the chloroacetic acid.