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Spaßige Übungen zur Nomenklatur in der Organischen Chemie
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Leni

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This document provides a comprehensive guide on Nomenklatur organischer Verbindungen Übungen (nomenclature exercises for organic compounds). It covers various types of organic compounds including alkanes, alkenes, alkynes, alcohols, aldehydes, ketones, carboxylic acids, and esters. The guide explains IUPAC-Nomenklatur rules and provides numerous examples and exercises for practice.

• The document begins with an overview of alkane nomenclature and structural formulas
• It then progresses to more complex organic compounds and their naming conventions
• Detailed explanations are provided for identifying longest chains, numbering carbons, and naming substituents
• The guide includes multiple practice exercises of varying difficulty levels
• Key concepts like functional groups, homologous series, and structural formulas are covered for different compound classes

3.3.2022

7696

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Nomenclature Exercises: Simple Formulas

This page presents a series of exercises focused on naming simple organic compounds, particularly alkanes with various branching patterns. The exercises are designed to reinforce understanding of IUPAC-Nomenklatur rules for naming organic compounds.

The page includes 17 structural formulas (A1 to A17) of increasing complexity, along with their correct IUPAC names. Some key examples include:

Example:

  • A1: H3C-CH2-CH3 (Propane)
  • A4: H3C-CH(CH3)-CH3 (2-Methylpropane)
  • A8: H3C-C(CH3)2-CH3 (2,2-Dimethylpropane)
  • A14: H3C-CH(CH3)-CH(CH3)-CH(CH3)-CH2-CH2-CH3 (2,3,4-Trimethylhexane)

The exercises progress from simple, unbranched alkanes to more complex structures with multiple methyl substituents.

Highlight: These exercises help students practice identifying the longest carbon chain, numbering carbons correctly, and naming substituents according to IUPAC rules.

Vocabulary: Substituents are groups attached to the main carbon chain, such as methyl (-CH3) or ethyl (-CH2CH3) groups.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Introduction to Organic Compound Nomenclature

This page introduces the basics of naming organic compounds, focusing on alkanes. It provides a list of the first ten alkanes in the homologous series from methane to decane along with their molecular formulas. The page also includes structural formulas for several alkanes to illustrate their bonding patterns.

Vocabulary: Alkanes are saturated hydrocarbons with single bonds between carbon atoms.

The page outlines the key steps for naming branched alkanes:

  1. Find and name the longest carbon chain
  2. Identify side chains (changing -ane to -yl)
  3. Determine how many of each side chain (di-, tri-, etc.)
  4. Number the longest chain to give side chains the lowest possible numbers
  5. List side chains alphabetically with their position numbers

Example: 4,6-Diethyl-2,6-dimethyloctane is given as an example of a complex alkane name.

The page concludes by mentioning alkenes (double bonds) and alkynes (triple bonds) as other hydrocarbon types.

Highlight: Understanding alkane nomenclature is fundamental for naming more complex organic compounds.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Aldehydes and Ketones

This page covers the nomenclature and structural characteristics of aldehydes and ketones, two important classes of organic compounds containing a carbonyl group (C=O).

Aldehydes:

  • The longest carbon chain is identified and named
  • The suffix -al replaces -ane in the name
  • Aldehydes always have a double-bonded oxygen at the end of the carbon chain

Example: Methanal, Ethanal, Propanal, Butanal

Ketones:

  • The longest carbon chain is identified and named
  • The suffix -one replaces -ane in the name
  • Ketones have a double-bonded oxygen within the carbon chain
  • Ketones only exist from propanone onwards (minimum 3 carbons)

Example: Propanone, Butan-2-one, Pentan-3-one, Cyclopentanone

Highlight: The key difference between aldehydes and ketones is the position of the carbonyl group - at the end for aldehydes and within the chain for ketones.

Vocabulary: The carbonyl group (C=O) is the defining feature of both aldehydes and ketones.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Alcohols and Their Nomenclature

This page focuses on the nomenclature of alcohols, which are characterized by the presence of at least one hydroxyl (-OH) group. The naming convention for alcohols involves changing the -ane ending of the parent alkane to -ol.

Definition: An alcohol is an organic compound with a hydroxyl (-OH) functional group attached to a carbon atom.

The page provides examples of different types of alcohols:

  1. Primary alcohol: Pentanol (Pentan-1-ol)
  2. Secondary alcohol: 2-Butanol (Butan-2-ol)
  3. Tertiary alcohol: 2-Methyl-2-Butanol

Vocabulary:

  • Primary alcohols have the -OH group attached to a carbon with one alkyl group
  • Secondary alcohols have the -OH group on a carbon with two alkyl groups
  • Tertiary alcohols have the -OH group on a carbon with three alkyl groups

The page also introduces the naming convention for compounds with multiple hydroxyl groups:

  • 2 OH groups: -diol
  • 3 OH groups: -triol
  • 4 or more OH groups: polyols

Highlight: The position of the hydroxyl group is indicated by a number in the name, showing its location on the carbon chain.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Nomenclature Exercises: Intermediate Formulas

This page continues with more challenging nomenclature exercises, focusing on alkanes with various alkyl group substituents and branched side chains. The exercises (B1 to B15) require a deeper understanding of IUPAC-Nomenklatur rules and the ability to identify more complex structural features.

Some notable examples from this set include:

Example:

  • B2: 4-Ethyl-2,3-dimethylheptane
  • B4: 2,3-Dimethyl-4,5-dipropylnonane
  • B7: 4-Ethyl-5-propyl-2,3,4,6-tetramethylheptane

These exercises introduce more diverse substituents such as ethyl, propyl, and butyl groups, as well as compounds with multiple types of substituents on the same molecule.

Highlight: The increasing complexity of these structures challenges students to carefully analyze the molecule, identify the longest chain, and correctly name and number all substituents.

Vocabulary:

  • Ethyl group: -CH2CH3
  • Propyl group: -CH2CH2CH3
  • Butyl group: -CH2CH2CH2CH3

The exercises also include examples of compounds where the choice of the main chain is not immediately obvious, requiring students to consider multiple possibilities to determine the correct IUPAC name.

Definition: The main chain in IUPAC nomenclature is the longest continuous carbon chain in the molecule, which forms the basis for the compound's name.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Advanced Nomenclature Exercises

This page presents the most challenging nomenclature exercises in the set, featuring highly branched alkanes with multiple types of substituents. These exercises (continuing from B11 to B15) require a mastery of IUPAC-Nomenklatur rules and the ability to analyze complex molecular structures.

Key examples from this advanced set include:

Example:

  • B11: 3,4-Diethyl-3,4,6-trimethyloctane
  • B14: 5-Butyl-4-ethyl-2,3,4,9-tetramethyl-6-propyldecan

These structures feature a combination of various alkyl groups (methyl, ethyl, propyl, butyl) attached to long carbon chains, often with multiple substituents on the same carbon atom.

Highlight: Solving these complex nomenclature problems requires careful analysis of the molecule's structure, consideration of all possible main chains, and correct application of substituent naming and numbering rules.

Vocabulary:

  • Diethyl: Two ethyl groups
  • Tetramethyl: Four methyl groups
  • Butyl: -CH2CH2CH2CH3 group

These exercises challenge students to:

  1. Identify the longest possible carbon chain
  2. Correctly number the chain to give substituents the lowest possible numbers
  3. Name all substituents and list them in alphabetical order
  4. Handle cases where there are multiple substituents of the same type (using prefixes like di-, tri-, tetra-)

Definition: In IUPAC nomenclature, when there are two or more chains of equal length that could be considered the main chain, the chain with the greater number of substituents is chosen as the main chain.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Carboxylic Acids and Esters

This page introduces the nomenclature and structural features of carboxylic acids and esters, two classes of organic compounds with important functional groups.

Carboxylic Acids:

  • The longest carbon chain is identified and named
  • The suffix -oic acid replaces -ane in the name
  • Carboxylic acids always have a carbonyl group (C=O) and a hydroxyl group (-OH) at the end of the carbon chain

Example: Methanoic acid, Ethanoic acid

Esters:

  • Named as alkyl alkanoates
  • The name consists of two parts: the alcohol portion and the acid portion
  • The suffix -oate is used for the acid part

Example: Propanoic acid ethyl ester

The page also provides a summary of naming conventions for various organic compound classes:

  • Alkenes: stem + ene
  • Alkynes: stem + yne
  • Alkanes: stem + ane
  • Aldehydes: stem + al
  • Ketones: stem + one
  • Alcohols: stem + ol
  • Carboxylic acids: stem + oic acid
  • Esters: acid stem + alkyl + oate

Highlight: Understanding the naming conventions for these functional groups is crucial for correctly identifying and naming organic compounds.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Öffnen

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Spaßige Übungen zur Nomenklatur in der Organischen Chemie

user profile picture

Leni

@leni_saul

·

33 Follower

Follow

This document provides a comprehensive guide on Nomenklatur organischer Verbindungen Übungen (nomenclature exercises for organic compounds). It covers various types of organic compounds including alkanes, alkenes, alkynes, alcohols, aldehydes, ketones, carboxylic acids, and esters. The guide explains IUPAC-Nomenklatur rules and provides numerous examples and exercises for practice.

• The document begins with an overview of alkane nomenclature and structural formulas
• It then progresses to more complex organic compounds and their naming conventions
• Detailed explanations are provided for identifying longest chains, numbering carbons, and naming substituents
• The guide includes multiple practice exercises of varying difficulty levels
• Key concepts like functional groups, homologous series, and structural formulas are covered for different compound classes

3.3.2022

7696

 

10

 

Chemie

212

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Nomenclature Exercises: Simple Formulas

This page presents a series of exercises focused on naming simple organic compounds, particularly alkanes with various branching patterns. The exercises are designed to reinforce understanding of IUPAC-Nomenklatur rules for naming organic compounds.

The page includes 17 structural formulas (A1 to A17) of increasing complexity, along with their correct IUPAC names. Some key examples include:

Example:

  • A1: H3C-CH2-CH3 (Propane)
  • A4: H3C-CH(CH3)-CH3 (2-Methylpropane)
  • A8: H3C-C(CH3)2-CH3 (2,2-Dimethylpropane)
  • A14: H3C-CH(CH3)-CH(CH3)-CH(CH3)-CH2-CH2-CH3 (2,3,4-Trimethylhexane)

The exercises progress from simple, unbranched alkanes to more complex structures with multiple methyl substituents.

Highlight: These exercises help students practice identifying the longest carbon chain, numbering carbons correctly, and naming substituents according to IUPAC rules.

Vocabulary: Substituents are groups attached to the main carbon chain, such as methyl (-CH3) or ethyl (-CH2CH3) groups.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Introduction to Organic Compound Nomenclature

This page introduces the basics of naming organic compounds, focusing on alkanes. It provides a list of the first ten alkanes in the homologous series from methane to decane along with their molecular formulas. The page also includes structural formulas for several alkanes to illustrate their bonding patterns.

Vocabulary: Alkanes are saturated hydrocarbons with single bonds between carbon atoms.

The page outlines the key steps for naming branched alkanes:

  1. Find and name the longest carbon chain
  2. Identify side chains (changing -ane to -yl)
  3. Determine how many of each side chain (di-, tri-, etc.)
  4. Number the longest chain to give side chains the lowest possible numbers
  5. List side chains alphabetically with their position numbers

Example: 4,6-Diethyl-2,6-dimethyloctane is given as an example of a complex alkane name.

The page concludes by mentioning alkenes (double bonds) and alkynes (triple bonds) as other hydrocarbon types.

Highlight: Understanding alkane nomenclature is fundamental for naming more complex organic compounds.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Aldehydes and Ketones

This page covers the nomenclature and structural characteristics of aldehydes and ketones, two important classes of organic compounds containing a carbonyl group (C=O).

Aldehydes:

  • The longest carbon chain is identified and named
  • The suffix -al replaces -ane in the name
  • Aldehydes always have a double-bonded oxygen at the end of the carbon chain

Example: Methanal, Ethanal, Propanal, Butanal

Ketones:

  • The longest carbon chain is identified and named
  • The suffix -one replaces -ane in the name
  • Ketones have a double-bonded oxygen within the carbon chain
  • Ketones only exist from propanone onwards (minimum 3 carbons)

Example: Propanone, Butan-2-one, Pentan-3-one, Cyclopentanone

Highlight: The key difference between aldehydes and ketones is the position of the carbonyl group - at the end for aldehydes and within the chain for ketones.

Vocabulary: The carbonyl group (C=O) is the defining feature of both aldehydes and ketones.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Alcohols and Their Nomenclature

This page focuses on the nomenclature of alcohols, which are characterized by the presence of at least one hydroxyl (-OH) group. The naming convention for alcohols involves changing the -ane ending of the parent alkane to -ol.

Definition: An alcohol is an organic compound with a hydroxyl (-OH) functional group attached to a carbon atom.

The page provides examples of different types of alcohols:

  1. Primary alcohol: Pentanol (Pentan-1-ol)
  2. Secondary alcohol: 2-Butanol (Butan-2-ol)
  3. Tertiary alcohol: 2-Methyl-2-Butanol

Vocabulary:

  • Primary alcohols have the -OH group attached to a carbon with one alkyl group
  • Secondary alcohols have the -OH group on a carbon with two alkyl groups
  • Tertiary alcohols have the -OH group on a carbon with three alkyl groups

The page also introduces the naming convention for compounds with multiple hydroxyl groups:

  • 2 OH groups: -diol
  • 3 OH groups: -triol
  • 4 or more OH groups: polyols

Highlight: The position of the hydroxyl group is indicated by a number in the name, showing its location on the carbon chain.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Nomenclature Exercises: Intermediate Formulas

This page continues with more challenging nomenclature exercises, focusing on alkanes with various alkyl group substituents and branched side chains. The exercises (B1 to B15) require a deeper understanding of IUPAC-Nomenklatur rules and the ability to identify more complex structural features.

Some notable examples from this set include:

Example:

  • B2: 4-Ethyl-2,3-dimethylheptane
  • B4: 2,3-Dimethyl-4,5-dipropylnonane
  • B7: 4-Ethyl-5-propyl-2,3,4,6-tetramethylheptane

These exercises introduce more diverse substituents such as ethyl, propyl, and butyl groups, as well as compounds with multiple types of substituents on the same molecule.

Highlight: The increasing complexity of these structures challenges students to carefully analyze the molecule, identify the longest chain, and correctly name and number all substituents.

Vocabulary:

  • Ethyl group: -CH2CH3
  • Propyl group: -CH2CH2CH3
  • Butyl group: -CH2CH2CH2CH3

The exercises also include examples of compounds where the choice of the main chain is not immediately obvious, requiring students to consider multiple possibilities to determine the correct IUPAC name.

Definition: The main chain in IUPAC nomenclature is the longest continuous carbon chain in the molecule, which forms the basis for the compound's name.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Advanced Nomenclature Exercises

This page presents the most challenging nomenclature exercises in the set, featuring highly branched alkanes with multiple types of substituents. These exercises (continuing from B11 to B15) require a mastery of IUPAC-Nomenklatur rules and the ability to analyze complex molecular structures.

Key examples from this advanced set include:

Example:

  • B11: 3,4-Diethyl-3,4,6-trimethyloctane
  • B14: 5-Butyl-4-ethyl-2,3,4,9-tetramethyl-6-propyldecan

These structures feature a combination of various alkyl groups (methyl, ethyl, propyl, butyl) attached to long carbon chains, often with multiple substituents on the same carbon atom.

Highlight: Solving these complex nomenclature problems requires careful analysis of the molecule's structure, consideration of all possible main chains, and correct application of substituent naming and numbering rules.

Vocabulary:

  • Diethyl: Two ethyl groups
  • Tetramethyl: Four methyl groups
  • Butyl: -CH2CH2CH2CH3 group

These exercises challenge students to:

  1. Identify the longest possible carbon chain
  2. Correctly number the chain to give substituents the lowest possible numbers
  3. Name all substituents and list them in alphabetical order
  4. Handle cases where there are multiple substituents of the same type (using prefixes like di-, tri-, tetra-)

Definition: In IUPAC nomenclature, when there are two or more chains of equal length that could be considered the main chain, the chain with the greater number of substituents is chosen as the main chain.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Carboxylic Acids and Esters

This page introduces the nomenclature and structural features of carboxylic acids and esters, two classes of organic compounds with important functional groups.

Carboxylic Acids:

  • The longest carbon chain is identified and named
  • The suffix -oic acid replaces -ane in the name
  • Carboxylic acids always have a carbonyl group (C=O) and a hydroxyl group (-OH) at the end of the carbon chain

Example: Methanoic acid, Ethanoic acid

Esters:

  • Named as alkyl alkanoates
  • The name consists of two parts: the alcohol portion and the acid portion
  • The suffix -oate is used for the acid part

Example: Propanoic acid ethyl ester

The page also provides a summary of naming conventions for various organic compound classes:

  • Alkenes: stem + ene
  • Alkynes: stem + yne
  • Alkanes: stem + ane
  • Aldehydes: stem + al
  • Ketones: stem + one
  • Alcohols: stem + ol
  • Carboxylic acids: stem + oic acid
  • Esters: acid stem + alkyl + oate

Highlight: Understanding the naming conventions for these functional groups is crucial for correctly identifying and naming organic compounds.

Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

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Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Kostenlose Lernzettel von Top-Schülern - Jetzt freischalten!

Kostenlose Notizen für jedes Fach, erstellt von den besten Schülern

Bekomme Noten mit intelligenter KI-Unterstützung

Lerne schlauer, weniger Stress - Jederzeit und überall

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Nomenklatur: Zeichnen & erkennen
Alkane
Methan (CH₂)
Ethan (C₂H6)
Propan (C3H8)
Butan (Cy H₁)
Pentan (Cs H₁₂)
Hexan (CoHin)
Heptan (CH)
Octa

Kostenlose Lernzettel von Top-Schülern - Jetzt freischalten!

Kostenlose Notizen für jedes Fach, erstellt von den besten Schülern

Bekomme Noten mit intelligenter KI-Unterstützung

Lerne schlauer, weniger Stress - Jederzeit und überall

Mit E-Mail anmelden

Mit der Anmeldung akzeptierst du die Nutzungsbedingungen und die Datenschutzrichtlinie

Nichts passendes dabei? Erkunde andere Fachbereiche.

Knowunity ist die #1 unter den Bildungs-Apps in fünf europäischen Ländern

Knowunity wurde bei Apple als "Featured Story" ausgezeichnet und hat die App-Store-Charts in der Kategorie Bildung in Deutschland, Italien, Polen, der Schweiz und dem Vereinigten Königreich regelmäßig angeführt. Werde noch heute Mitglied bei Knowunity und hilf Millionen von Schüler:innen auf der ganzen Welt.

Ranked #1 Education App

Laden im

Google Play

Laden im

App Store

Knowunity ist die #1 unter den Bildungs-Apps in fünf europäischen Ländern

4.9+

Durchschnittliche App-Bewertung

13 M

Schüler:innen lieben Knowunity

#1

In Bildungs-App-Charts in 12 Ländern

950 K+

Schüler:innen haben Lernzettel hochgeladen

Immer noch nicht überzeugt? Schau dir an, was andere Schüler:innen sagen...

iOS User

Ich liebe diese App so sehr, ich benutze sie auch täglich. Ich empfehle Knowunity jedem!! Ich bin damit von einer 4 auf eine 1 gekommen :D

Philipp, iOS User

Die App ist sehr einfach und gut gestaltet. Bis jetzt habe ich immer alles gefunden, was ich gesucht habe :D

Lena, iOS Userin

Ich liebe diese App ❤️, ich benutze sie eigentlich immer, wenn ich lerne.