Name each of the following compounds. Then draw the compound and one isomer of each compound. (Isomer classes indicated)
(NH4)4[Fe(ONO)6], Linkage
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Name each of the following compounds. Then draw the compound and one isomer of each compound. (Isomer classes indicated)
For each of the following compounds, draw a geometric isomer if one exists. thank you CI
INSTRUCTIONS: For each of the following organic molecules, you will do the following. A. Draw the expanded form of the organic compound. B. Name your organic compound. For organic compounds, #3-7 in addition to instructions 1 and 2, you need to also do the following. D. Label each carbon as primary, secondary, tertiary or quaternary E. Draw the skeletal form of the organic molecule. 1. Organic Compound: CH Structure: name: 2. Organic Derivative: CH,CI Structure: name: 3. Organic Compound CaH...
5. State the number of isomers that exists for the following complexes, name each type of isomer and draw the structure of the isomers: (8 points) Number of possible isomers Structure of each type and Name a. [Co(NHa)4Fl b. [Fe(H20)2Cla] c. [Pt(NHs)2Cl2] d. [Fe(CO)s(NH3)3]3 5. State the number of isomers that exists for the following complexes, name each type of isomer and draw the structure of the isomers: (8 points) Number of possible isomers Structure of each type and Name...
. Consider the three isomers of the trichlorinated benzene compound, C6H3Cl3. (a) Draw each isomer, name it and determine its point group. (b) Using ONLY the C-Cl bonds as a basis set, determine C-Cl for each system and break it down into the corresponding irreducible representations. (c) For each isomer, indicate how many IR and Raman Peaks should be observable corresponding to the C-Cl stretching frequency. Perhaps a table to summarize your results would be appropriate.
4. Consider the following compound with the molecular formula C4H:02: a. Draw a constitutional isomer that you expect will be approximately one trillion (1012) times more acidic than the compound above. b. Draw a constitutional isomer that you expect will be less acidic than the compound above. c. Draw a constitutional isomer that you expect will have approximately the same pKa as the compound above.
0,5. Draw structure and make models for only one isomer of the following compounds. a) C4H80 (an aldehyde) b) C2H4O2 (a carboxylic acid) c) C5H100 (an alkene and an ether) d) CsH100 (a ketone) c) CsH100 (an alkene and an alcohol
The systematic (IUPAC) name for one of isomers is butanal. Draw the structure of this isomer: Edit Hąc * Incorrect. Draw the structure of the remaining isomer: HC Edit
Correctly name the compounds or write the formulas. Identify each compound as molecular, fixed-charge ionic, variable-charge ionic, hydrate, binary acid, or oxyacid. Each compound falls into only one category. Formula Name Category cerium (III) arsenate V,(Cr, 0,), potassium tungstate As,o, nickel (III) phosphate heptahydrate Correctly name the compounds or write the formulas. Identify each compound as molecular, fixed-charge ionic, variable-charge ionic, hydrate, binary acid, or oxyacid. Each compound falls into only one category Formula Name Category diboron hexahydride (NH,C,D, iron...
8.1) 8.5) Give the appropriate IUPAC name for the following structural formula of a halogenated compound. CH3 CI Нас (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis/trans designations only to represent stereochemistry for cyclic compounds. It is not necessary to use italics in writing compound names.) Name: There are five cycloalkanes with the molecular formula C5H10. When treated with chlorine at 300°C, isomer A gives one monochlorination product. Under the same conditions, isomer B...
1. Consider an organic compound with molecular formula C H:02: a) Draw one constitutional isomer that has a very small pka. b) Draw a constitutional isomer that is less acidic than the compound from part a). c) Draw a constitutional isomer that has is more basic than the compound in part b). D J AL . ... .... . . .. . . - Predict the stracture of the product formed in the reaction of 3-(3-5cetyl-5-for myl-4- hydroxy Phenyi) Propohoic...