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A: # First we have to know about constitutional isomerism : Consitutional isomerism : Those compounds…
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Q: What is the IUPAC name for the above?
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Q: Name the following using IUPAC nomenclature. CI
A: IuPAC name should be assigned by following some rules.
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Q: C a e
A: Alkyne = Alkyne are Unsaturated Hydrocarbon containing atleast one carbon-carbon Triple bond (C≡C)…
Q: F
A: IUPAC NomenclatureInternational union of pure and applied chemistry nomenclature , by this…
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A:
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Q: NO,
A: Given,
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A: The longest carbon chain i.e parent chain in the molecule is of 8 carbon as shown below.
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A: IUPAC NAMES of following compounds are
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A: IUPAC naming: It can be define as a method in which naming of the organic compound is done based on…
Q: name the following molecule with the correct IUPAC name
A: In nomenclature, the IUPAC nomenclature of chemistry is a method of naming organic chemical…
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- A. Structural Isomerism of Alkanes, continued. Construct models for the five alkanes that have the molecular formula C6H₁4. All five of your models should have the same number of each type of atom, but they should have the atoms connected in a different order. Thus the molecules they represent are structural isomers of one another. Note the tetrahedral geometry of each carbon atom. Draw an extended and a condensed structure (NOT skeletal/line angle) of each structural isomer, then determine its IUPAC name. Recall that since the IUPAC name specifies the number of each type of atom and how they are connected, each structural isomer will have a different name. Each name should very specifically describe the structure. Isomer 3: Extended Structure Isomer 3: Condensed Structure IUPAC Name: IUPAC Name: Isomer 4: Extended Structure Isomer 4: Condensed StructureCondensed structural formula of:1. neopentane 2. n-hexane3. 2-Ethyl-1,4-dimethylcyclopentane4. chloroform5. 2-Bromo-1-chloro-3-ethyl-2,3,5-trimethylheptane2. Identify the functional groups labelled A-I. HO, CO2H HOʻ но. HO, CO2H A HO H „CH3 H3č „CH3 H H3C° но E F Zocor (Merck) Pravachol (Bristol-Myers Squibb) Lipitor (Pfizer) FUNCTIONAL GROUPS A. В. C. D. Е. F. G. Н. I.
- 1. Name the following alkyl halides (hydrocarbons with halogens) following the example glven. The example is shown as both condensed and skeletal structure for reference. Note that chloro is listed before methyl (alphabetical order). CH,CH,CHCH,CI CH, 1-chloro-2-methyl-butaneLine-bond structures appear to imply that there are two different isomers of 1,2-dibromobenzene, one with the bromine-bearing carbon atoms joined by a double bond and one with the bromine-bearing carbons joined by a single bond. In fact, though, there is only one 1,2-dibromobenzene. Explain. H H. C. Br H. .C. Br || || .C and 1,2-Dibromobenzene Br BrDraw an acceptable Lewis structure from each condensed structure, such that all atoms have zero formal charge. a. diethyl ether, (CH3CH2)2O, the rst general anesthetic used in medical proceduresb. acrylonitrile, CH2CHCN, starting material used to manufacture synthetic Orlon bersc. dihydroxyacetone, (HOCH2)2CO, an ingredient in sunless tanning productsd. acetic anhydride, (CH3CO)2O, a reagent used to synthesize aspirin
- 3. Which of the following does not show conformational isomerism and Explain the reason for each? A. Ethane B. Ethene C. Ethyne D. Methane. 5. Why conformational isomers generally can not be separated from one another at room temperature?8. Circle and label all functional groups in the following molecules. a. b. C. d. HO H- _i___._. H₂ HO H3C C HN H₂C -CH3 H₂ -0-CH3 CH3 H CH3I. Molecule's Degree of Unsaturation* *to avoid confusion, we shall use "degree of unsaturation" to refer to the number of pi bonds or number of rings present in the molecule as a result of the loss of hydrogen atoms when referenced using the alkane formula of C,„H2n+2" The numerical value for the degree of unsaturation = 1 means that a molecule of hydrogen, H,, or two atoms of hydrogen are lost and instead 1 pi bond OR 1 ring is seen in the molecule. For this exercise, determine the degree of unsaturation of each of the following compounds: CH3 1. 2,3,3-Trimethyl-1,4,6-octatriene CH3 6. CH3 2. 3-Ethyl-2,2,-dimethyl-3-heptene `CH3 3. 2-Methyl-1,5-hexadiene 8. 7. ÇH3 H. CH3 4. 4-tert-Butyl-2-methylheptane Answers: 1. L2. 3. _4. 5. 6. _7. 8. 5.