What is the IUPAC name for the compound shown? Step 2: What is the base name or parent name of Step 1: Identify the the molecule? number of carbons in dodecane the longest chain decane Step 2: Identify the base name of octane the molecule. nonane Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name.

What is the IUPAC name for the compound shown? Step 2: What is the base name or parent name of Step 1: Identify the the molecule? number of carbons in dodecane the longest chain decane Step 2: Identify the base name of octane the molecule. nonane Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

What is the IUPAC name for the compound shown? Step I: Identify the number of carbons in the longest chain Step 2: Identify the base name of the molecule. Step 3: Number the longest chain. Step 4: Identify substituents. Step 5: Order the substituents. Step 6: Add the substituent locants or numbering. Step 7: Put it all together and give the IUPAC name. Step 4: Identify the substituents in the molecule. A. How many methyl substituents are in the compound? B. What prefix is needed for the methyl substituents? C. What are the remaining substituents? ethyl pentyl propyl butyl
Match the organic compounds with its name. Match each item to a choice: Choices: # 3-ethyl-3,5-methyloctane # 2-methyl-1,3-butadiene # 1,1-dimethylhexane # 3-ethyl-3,5-dimethyloctane i 4,4-dimethylcycloheptene i 3,3,7-trimethyldecane # 4-ethyl-2,2-dimethylheptene : 1,1-dimethylcyclohexane | 2-ethyl-2,6-dimethylnonane i 4-ethyl-2,2-dimethyl-3-heptene
Alkanes are hydrocarbons containing only single bonds. How many hydrogen atoms are in an acyclic alkane with 8 carbon atoms? H atoms: How many hydrogen atoms are in an acyclic alkane with 16 carbon atoms? H atoms:
When numbering the carbons in alkenes or alkynes, Question 7 options: The carbon that contains the first branch is numbered carbon 1. It does not matter where you begin numbering. The location of the multiple bond takes precedence There is no system in place for this.
Draw the constitutional isomers of the molecular formula C8H18 and name each using IUPAC system. a. Which one gives two and only two monobromo derivatives when it reacts with Br2 and light? Name the products using IUPAC system b. Which give three and only three monobromo products? Name the products, using the IUPAC system.
Determine whether the compound is an alkene, alkyne, alcohol, or ethe
So, this is one of the questions on our quizzes. As far as I know, it's supposed to be 2-diethyl-5-methylhexane but it's not in the choices. Correct me if I am wrong. The quiz is about IUPAC naming of alkanes.
Which statement is true with reference to the halogenation of an alkane? Question 8 options: Halogenation of alkane forms an alkene and HX (where X represents an halogen atom) Halogenation of alkane forms an alkyl halide and HX (where X represents an halogen atom) Halogenation of alkane forms an alkyne and HX (where X represents an halogen atom) Halogenation of alkane forms an alcohol and HX (where X represents an halogen atom)
What is the difference between a saturated hydrocarbon and an unsaturated hydrocarbon? Unsaturated hydrocarbons have no multiple covalent bonds. The unsaturated hydrocarbon has at least one multiple covalent bond. Unsaturated hydrocarbons must not have cis/trans isomers O Unsaturated hydrocarbons must have at least two atoms joined by bonds that can rotate