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Chapter 10: Problem 80

The correct IUPAC name of the following compound is (a) \(5-\left(1^{\prime}, 1^{\prime} 2^{\prime}\right.\) -trimethyl propyl)-2-2-dimethyl nonane (b) 4 -Butyl- \(2,3,3,7,7\) -pentamethylnonane (c) \(2,3,3,7,7\) -Pentamethyl-4-butyloctane (d) 2,2-Dimethyl-5-(1', \(1^{\prime}, 2^{\prime}\) trimethylpropyl)nonane

Short Answer

Expert verified
The correct IUPAC name is (d) 2,2-Dimethyl-5-(1',1',2'-trimethylpropyl)nonane.

Step by step solution

01

Identifying the Longest Carbon Chain

To determine the correct IUPAC name, start by finding the longest continuous carbon chain in the compound. In the options provided, the main chain consists of nonane, indicating a nine-carbon chain. Review options and ensure they match this identification.
02

Identifying Substituents

Check the substituents attached to the longest carbon chain. In the given options, substituents include groups such as dimethyl, butyl, and trimethylpropyl. Properly identify each based on common IUPAC naming conventions.
03

Assigning Correct Positions to Substituents

Assign numbers to the carbon atoms in the longest chain such that substituents receive the lowest possible numbering. Examine the options and verify correct positioning as per IUPAC rules: prioritize smaller numbers for substituents and larger substituents over smaller.
04

Drawing and Comparing Structures

Draw the structure of each option using IUPAC naming rules, then compare them. Identify any discrepancies in the naming, such as incorrect parent chain identification or incorrect substituent positioning.
05

Choosing the Correct Name

After verifying the correct numbering and identification of substances according to IUPAC rules among the options, determine which name correctly describes a nonane with substituents: dimethyl and a 1',1',2'-trimethylpropyl group. Verify consistency with IUPAC guidelines.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Longest Carbon Chain
When it comes to naming organic compounds using the IUPAC system, the first crucial step is identifying the longest continuous carbon chain. This chain will form the foundational backbone of the compound's name. In the case of the exercise, the longest carbon chain is nonane, meaning it is made up of nine carbon atoms. Here鈥檚 how you can do it:
  • Count the carbon atoms in the continuous chain.
  • Ensure no shortcuts鈥攇o straight through without skipping any carbons.
  • Re-evaluate if necessary to confirm the longest possible main chain.
Finding this main chain is vital as it determines the base name and heavily influences numbering and substituent labeling. Remember, accuracy is key in distinguishing subtle differences that can change the meaning, thus affecting IUPAC correctness.
Substituent Identification
After pinpointing the longest carbon chain, the next step is to identify the substituents attached to it. Substituents are groups or atoms attached to the main carbon chain that are not included in the primary chain itself. In the exercise, substituents such as dimethyl, butyl, and trimethylpropyl appear.
  • Carefully mark all groups branching from the main carbon chain.
  • Classify each based on structures, often using common termini like 'methyl', 'ethyl', 'propyl', etc.
This stage is crucial for the precise description of the molecule's overall structure. Have a keen eye, as mistakes in this step could lead to incorrect naming. Each substituent needs a name鈥攖ypically derived by adding prefixes for the quantity of similar groups and suffixes, like 'yl', indicating its branching nature.
IUPAC Naming Conventions
Naming using the IUPAC convention can seem daunting at first, but it becomes straightforward once you understand the guidelines. In this exercise, following the standardized IUPAC naming rules ensures consistency across the board. The key aspects include:
  • Longest Chain Determines Base Name: Identify the main chain as previously discussed, assigning its name appropriately based on the number of carbons (e.g., 'nonane' for nine carbons).
  • Numbering the Chain: Use numbers to specify the position of groups; they must receive the lowest possible numbers to maintain order.
  • Alphabetical Order of Substituents: When multiple different substituents are present, arrange them alphabetically in the name (ignoring prefixes like di, tri, etc., for alphabetical purposes).
Understanding these rules helps in constructing names that are universally recognized, minimizing confusion and ensuring detailed chemical communication.
Carbon Chain Numbering
Correctly numbering the carbon chain is pivotal for IUPAC nomenclature. This is because it dictates the exact location of substituents along the chain, impacting the final name. To number the carbon chain:
  • Number consecutively from the end of the chain that provides substituents with the lowest positional numbers possible.
  • Choose the numbering scheme that favors the emergence of crucial substituents first, primarily if ties occur.
  • Re-assess if an alternative route allows for better alignment with IUPAC rules.
In the exercise, ensuring numbers align with the chemical structure鈥檚 substituents, such as the positioning of dimethyl, butyl, and trimethylpropyl groups, ensures the name's viability. This intricate step secures the precision required in chemical nomenclature, reducing misunderstanding in chemical identification.

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Most popular questions from this chapter

Which statement is correct in the following? (a) Alicyclic compounds are acyclic compounds. (b) In secondary amine, nitrogen is attached to \(2^{\circ}\) carbon atom. (c) \(1^{\circ}, 2^{\circ}, 3^{\circ}\) amines are homologues of each other. (d) \(\mathrm{HCOOCH}_{3}\) and \(\mathrm{CH}_{3} \mathrm{COOH}\) are not homologues of each other

The organic compound (Cyclohex-3-enyl) 2 -ethyl cyclobutanecarboxylate does not contains (a) two \(3^{\circ}\) -carbon atoms (b) two \(1^{\circ}\) -carbon atoms (c) 9 secondary \(\mathrm{C}\) -atoms (d) one \(1^{\circ}\) -carbon atoms

Identify incorrect matching in the following (a) Allyl alcohol-Prop-2-en-1-ol (b) Vinyl alcohol-Ethenol (c) Propargyl alcohol-But-3-yn-1-ol (d) Acrylaldehyde-2-Propenal

The IUPAC name of (a) N-Cyclohexylbenzamide (b) N-Phenyl-N-cyclohexylmethanamide (c) N-phenylcyclohexane carboxamide (d) N-Cyclohexyl-N-phenylmethyl amide

(S)-(N,4)-dimethyl-3-aminopentan-2-one
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