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need help naming and drawing this molecule 1. (4 points) Give the correct IUPAC name for the following molecul draw the expanding structure. (CH3)3C(CH2)3C(i-C3H7) (C2 Hs) (s-C4 Hg) a) C CH C
1. Naming and Drawing Carboxylic Acids: 1.A. Using IUPAC guidelines, enter the name for the carboxylic acid shown below. Enter the name using IUPAC guidelines, including numbers and punctuation (e.g., 3,4-dichlorobenzoic acid). 1.B. Draw 3-methylbenzoic acid. (Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Include all hydrogen atoms). 2. Naming Carboxylic Acid Derivatives: 2.A. Give the IUPAC name of the ester shown....
Worksheet: Naming and Drawing Alkanes For each alkane write the correct IUPAC name For each, draw a structural diagram (line, condensed or complete) 1. 2-methypentane 2. 2,3,4-trimethylheptane 3. -butyl-6-cthyl-2.5-dimethylnonane 4. Octane 5. 2,3-dimethylbutane 6. 3,3-dimethylhexane 7. 3-ethyl-3-methylhexane 8. 5.5-diethyl-2.2.44-tetramethyloctane
Drawing and naming structural isomers 1. A C6H14 compound that gives two C6H13Cl structural isomers 2. Two different C6H14 compound that gives three different C6H13Cl isomers
is this correct? Data Table Part A. Drawing Formulas and Naming Hydrocarbons. Name: 3-methylpentane Name: 2,3-dimethylhexane 5-pentand 6-an CH3 Name: 11-dimethylcyclohexane CHE Name: 3-cloro 2-methylpe CI CHE - CH₃ CH3-CH2=CH-CH-C 2-methyl Name: 3-methylcyclopentene Name: 2,3-dibromo-1-butene Br Name: Name: 3-methyl-1-butyne CH,CHCH= CHCH,CH3 CH3 Name: 4-bromo-3-chloro-1-heptyne Name: CH, CH,-cácc=CH-C CH3 CH3
LasoRATO 11 vEPR w aD MoLECULAa GeoMETY EXAMPLE PROBLEM: DRAWING AND NAMING VSEPR STRUCTURES TABLE 2 Electron Units on Central Molecular Geometry (Number of Lone Pairs around the Central Atom) Electron Geometry Atom 2 3 3 5 _ CHEM 111 155
naming compounds
Acid hydrolysis of amides one of the most used methods in the synthetic transformation of amides to carboxylic acids. Provide a stepwise mechanism of the transformation below H20, Ht NH2 OH
2. Acid hydrolysis of amides one of the most used methods in the synthetic transformation of amides to carboxylic acids. Provide a stepwise mechanism of the transformation below. НаО, Н* NH2 "ОН
Pka and structure of various amides. I need some help better understanding primary, secondary, and alpha-amides associated with the following pka values. I got these values from our class pka chart. Primary amide pka = 15, Seccondary amide pka = 15, alpha-amide pka =25. Particularly, I need help seeing how the alpha-amide is different structurally (molecular structure and/or lewis strucutre) than the primary amide. Thanks!