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- 2. A student named a compound as 6-methyl-6-ethylhept-1-en-5-one. Even though one can draw a correct structure based on that name, the name itself is incorrect according to the IUPAC naming conventions. Draw a structure for the compound (based on the above name), and then name the compound correctly. Structure Correct NameDraw a structure a. 3,4-dimethylpent-1-yneb.3-methyl-3-ethyl-1-butenec. 3,3-dimethyl-4-decened.1,1-dimethyl-4-ethyl-2,5-cyclohexadienee. 4-ethyl-2,3-dimethyl-2-heptenef. 1-chlorocyclopropeneg. 2,6-dimethyl-2,5-octadieneh. 1-cyclobutyl-3-methyl-1-butynei. 5-bromo-2-chlorotoluene1. What is the correct IUPAC name for 5-butyl-6-ethyl-4-methylhex-1-ene (For Alkene and Alkyne Naming, follow this format “Branch-Carbon Prefix-Functional Group Suffix”) e.g. 3-methylhex-2-ene 2. What is the correct IUPAC name for 3,4-dimethylhex-5-ene-1-yne
- 1. What is the correct IUPAC name for 2-propylpentane (For Alkene and Alkyne Naming, follow this format “Branch-Carbon Prefix-Functional Group Suffix”) e.g. 3-methylhex-2-ene 2. What is the correct IUPAC name for 3-butyl-2-isopropylpentane 3. What is the correct IUPAC name for 2,5-Dipropylhexane 4. What is the correct IUPAC name for 5-butyl-6-ethyl-4-methylhex-1-ene 5. What is the correct IUPAC name for 3,4-dimethylhex-5-ene-1-yne6. Complete the following reactions for alkynes. Draw the structure of the product. Name the reactant and the product. a) b) c) CH3 I CH-CECH CH3 CH₂-CH-CH ett₂ C=CH CH₂-CH-CH3 CH₂₂ CH + 2Br₂ + 1Br₂ + 2HCIYou are trying to monochlorinate 2,4,4-trimethylhexane to form a compound with the molecular formula C9H19Cl. Answer following question: A. Draw the structures of all the monochlorinated isomers which have the formula C9H19Cl and are derived from 2,4,4-trimethylhexane. B. Give the IUPAC name for each of the structures you drew in part A. C. For each of the structures you drew in part A circle any asymmetric carbon atoms.
- How could 2,6-dimethylheptane be prepared from an alkyne and an alkyl halide? (The prime in R′ signifies that R and R′ can be different alkyl groups.)draw the skeletal (line-bond) structure of (S)-2-bromo-4-ethylhexane. please be sure to read molecule correctly, I saw someone ask this same question but the homework helper but Methylhexane instead of ethylhexane.1.Draw a structure that corresponds to the incorrectly named: 6-tert-butyl-3-isopropylhexane. 1b. Rename the compound above according to the IUPAC rules. 1c. Draw a circle around every methine (3o) carbon and a square around every 4o carbon. How many 1o and 2o carbons arepresent?
- i Ii. In. * e A M 1:-r CH3-CH-CH2-CH-CH3 C2H5 Br 2-bromo-4-methylhexane 2-bromo-4-ethylpentane This compound CH3CH2CH is primary carbon secondary carbon tertiary carbon اكتب اسمك الرباعي بال لغه العربيه إجابتك * Weak acid has Ka is less than 1 true False IIC. Draw the structure of the following compound. 1. 3-[(methyltio)methyl]-1-cyclohexene 2. 2,3-Dihydro-1,4-dithianaphthalene 3. 2,3-Epithiohexane1. Explain the following - why stearic acid has higher melting point than decanoic acid. - why benzoic acid has higher melting point than stearic acid. - why salicylic acid has higher melting point than benzoic acid. - why octane has a higher melting point than isooctane. - why 2,2,3,3-tetramethylbutane has the highest melting point among the three isomers of C8H18.