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Represents the proportion of questions from this topic.
Yearly Question Distribution
Year
Topic Area
Concepts Covered
Number of Questions
Difficulty Level
Key Focus Areas
2024
IUPAC Nomenclature
IUPAC Nomenclature
1
Easy
IUPAC naming rules and conventions
2023
-
-
-
-
-
2022
-
-
-
-
-
2021
Isomerism in organic compound/Tetravalence of carbon
Metamerism/ Hybridisation
1
Easy
Understanding different types of isomerism and carbon’s valence structure
2020
Qualitative and Quantitative Analysis / Fundamental concepts in Organic Reaction Mechanism
Extraction of mixture of Organic Compounds / Chromatography / stability of carbocation
1
Difficuit
Separation techniques and reaction mechanisms
2019
Nomenclature of Organic Compounds
IUPAC Nomenclature
1
Easy
Systematic naming of organic compounds
2018
-
-
-
-
-
2017
Nomenclature of Organic Compounds/Fundamental Concepts in Organic Raction Mechanism
IUPAC nomenclature / Nature of Electrophiles / Resonance
1
Easy
Nomenclature rules and basic reaction concepts
Related Video
IUPAC Nomenclature System Study Notes
Table of Contents
Introduction to Nomenclature Systems
Trivial System
IUPAC Nomenclature System
3.1 Evolution of IUPAC System
3.2 Functional Group Indicators
3.3 Priority Order of Functional Groups
Functional Group Naming Conventions
Summary
1. Introduction to Nomenclature Systems
Key Concepts
Nomenclature is the systematic naming of chemical compounds.
Two primary systems exist: Trivial System and IUPAC System.
The Trivial System relies on common names assigned arbitrarily, while the IUPAC System provides a standardized, structural-based naming convention.
Definitions
Common Names: Names assigned by discoverers without a systematic basis. Systematic Names: Names derived from structural analysis, standardized by IUPAC.
2. Trivial System
Key Points
Arbitrary Naming: Names were assigned based on discoverer preference, leading to inconsistencies.
Examples:
Acetic acid (common name for CH₃COOH)
Benzene (common name for C₆H₆)
Limitations: Lack of universal rules and potential ambiguity.
3. IUPAC Nomenclature System
3.1 Evolution of IUPAC System
1957: The International Union of Pure and Applied Chemistry (IUPAC) established a systematic approach for naming organic compounds.
Objective: Ensure clarity, consistency, and universal applicability based on molecular structure.
3.2 Functional Group Indicators
Prefixes: Used for functional groups with higher priority (e.g., “hydroxyl” for -OH).
Suffixes: Used for functional groups with lower priority (e.g., “-ane” for alkanes).
Examples:
Alcohols: “Alcohol” as a suffix (e.g., ethanol).
Carboxylic Acids: “Oic acid” as a suffix (e.g., acetic acid).
4. Functional Group Naming Conventions
Key Rules
Highest Priority First: The functional group with the highest priority dictates the suffix.
Alphabetical Order: Prefixes are ordered alphabetically, ignoring “hydro” or “oxy” prefixes.
Examples:
2-Phenylbutanoic Acid:
“Phenyl” (prefix) indicates an aromatic ring.
“Butanoic acid” (suffix) denotes the carboxylic acid functional group.
Special Cases
Cyclic Compounds: Use “cyclo-” prefix (e.g., cyclohexane).
Multiple Functional Groups: Use prefixes for multiple groups (e.g., “hydroxylamino”).
5. Summary
Key Concepts
Trivial System: Arbitrary names with no systematic basis.
IUPAC System: Systematic, structural-based naming standardized by IUPAC.
Functional Groups: Indicated by prefixes or suffixes based on priority.
Priority Order: Functional groups are ranked to ensure consistent naming.
##### In which of the following functional group isomerism is not possible?
1. [ ] Alcohols
2. [ ] Aldehydes
3. [x] Alkyl halides
4. [ ] Cyanides
##### Identify the compound that exhibits tautomerism
1. [ ] 2-Butene
2. [ ] Lactic acid
3. [x] 2-Pentanone
4. [ ] Ethane
##### The number of stereoisomers possible for a compound of the molecular formula $CH_3-CH=CH-CH(OH) Me$ is
1. [ ] 3
2. [ ] 2
3. [x] 4
4. [ ] 6
##### 3-Methylpent-2-ene on reaction with $HBr$ in presence of peroxide forms an addition product. The number of possible stereoisomers for the product is
1. [ ] Six
2. [ ] Zero
3. [ ] Two
4. [x] Four
##### Which of the following compound will exhibit geometrical isomerism?
1. [x] 1-Phenyl-2-butene
2. [ ] 3-Phenyl-1-butene
3. [ ] 2-Phenyl-1-butene
4. [ ] 1,1-Diphenyl-1-propane
##### Which of the following compounds will show metamerism?
1. [ ] $HCOOCH_3$
2. [x] $C_2 H_5-S-C_2 H_5$
3. [ ] $CH_3 -O-CH_3$
4. [ ] $CH_3-O-C_2 H_5$
##### Nitroethane can exhibit one of the following kind of isomerism.
1. [ ] Metamerism
2. [ ] Optical activity
3. [x] Tautomerism
4. [ ] Position isomerism
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