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For the following acid hydrolysis reaction; Trans-[Co(en)2Cl2]+ + H2O cis- and trans-[Co(en)2(H2O)Cl]2+ a) Write the rate equation. b) How can you calculate the activation enegry? Explain briefly.
1. Using the concept of trans activating ligands, predict the following reaction products (A, B, C, D, E, F) Hint: Cl- is greater than py in trans activation.a. [PtCl4]2- + CN- → A + NH3 → B + py → C b. [PtCl4]2- + NH3 → D + CO → E + py → F
Organic Chemistry Addition of Bromine to an Alkene-HELP ASAP PLEASE table of reagents and properties Reagent MW (g/mol) mp(Celsius) d( g/ml) trans-cinamic acid 148.2 132-135 acetic acid 60 1.05 pyridinium tribromide 319.8 - 2,3-dibromo-3-phenylpropanoic acid 308.0 Pair A: 93-95, Pair B: 202-204 Organic Chemistry- addition of bromine to an Alkene For a lab the preparation of 2,3-dibromo-3 phenylpropanoic acid was done. 1.2 g of trans-cinnamic acid was dissolved in 4 ml of glacial acetic acid. 2.5 g of pyrimide tribromide...
ORGANIC CHEMISTRY II (CHE251) written Homework Assignment #9-Due Thursday, 4125 at 12:30 PM Suffolk County Community College Ammeman Campus Department of Physical Science 2. Write an lUPAC name for each amide. Begin by witing the name of the parent carboxylic acid. Be sure to include all necessary stereochemical designations (cis, trans, E, Z, R, S), (3 pts) Parent Carboxy ic Acid Name: Amide Name Parent Carboxylic Acid Name Amide Name: Parent Carboxylic Acid Name Amide Name: 3. Write an IUPAC...
a) When [Ni(NH3)4]2+ is treated with HCl, two compounds having the formula [Ni(NH3)2Cl2] (designed X and Y) are formed. X can be converted into Y by diluting in dilute HCl. A solution of X reacts with oxalic acid to form Z complex [Ni(NH3)2C2O4], Y does not react with oxalic acid. Identify X, Y and Z complexes and draw the geometrical structure of them.b) In an unlabelled bottle, it is known to contain potassium diaquadioxalatochromate(III) complex in it. How can...
This is an organic chemistry question regarding the Diels-Alder reaction. The problems are 16.22 and 16.18. I would like to know if I did these correctly. If I did not, could someone help me go through the process? er reaction Conjugation, Resonance and Dienes Chapter 16 dienophile react in a Diels-Alder CH3 C. 16.18 Draw the product formed when each diene and Problem 16.18 COOCH3 15 Specific Rules Governing the Diels-Alder Reaction 16.13A Diene Reactivity Rule [1] The diene can...
Organie Chemistry Organic Chem . Organic Nomenclature Chemistry Organic Chemistry Problems Of Alkenes Name Joshelyo Palma Dato Problem 1: Are the following alkenes circle the carbon.carbon double bond and clearly indicate if the alkene is cis, trans or neither? Problem 2: Use the labels E and Z to best describe the stereochemistry of the alkenes below. а) ОН NH2 HN, с Problem 3: Using IUPAC rules name the following molecules. wawa (E) 2-hexene (26,45)-2,4-hexadiene (27,4E-2, 4-hexadiene (2.5, us)-4-methyl-2-hexe Organic Chemistry...
Klein, Organic Chemistry, 2e For each of two eoisomers of 1,3-dimethylcyclohesane 1,3-d one Haworth and two chair conformations are appropriate Your answer is incorrect. Try again. Choose correct statements. (Several choices may be correct.) corresponds to Haworth projection of cis-1,3-dimethylcyclohexane H3 corresponds to Haworth projection of trans-1,3-dimethylcyclohexane corresponds to Haworth projection of cis-1,3-dimethylcyclohexane corresponds to Haworth projection of cis-1,3-dimethylcyclohexane carresponds to Haworth projection of trans-1,3-dimethylcyclohexane. corresponds to Haworth projection of trans-1,3-dimethylcyclohexane
inorganic chemistry 1) trans-FeCl2(dppe)2 is a green colored compound. Upon reduction of this coordination compound with NaBH4, and orange colored trans-FeH2(dppe)2 results. Explain the origin in the difference of colors by drawing a d-orbital splitting diagram for each complex.
inorganic chemistry 1) trans-FeCl2(dppe)2 is a green colored compound. Upon reduction of this coordination compound with NaBH4, and orange colored trans-FeH2(dppe)2 results. Explain the origin in the difference of colors by drawing a d-orbital splitting diagram for each complex.