alkanes
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Questions and Answers

What is the role of the electronegative leaving group in a substitution reaction?

  • To stabilize the electrons it leaves with
  • To attract the electrophile
  • To create a partial charge to attract the positive charge of the nucleophile
  • To create a partial charge to attract the negative charge of the nucleophile (correct)
  • What is the second key criterion for a leaving group?

  • To stabilize the electrons it leaves with (correct)
  • To be an electron pair acceptor
  • To be a bromine atom
  • To create a partial charge to attract the nucleophile
  • What is the general term for a compound where a carbon group is bonded to a halide?

  • Haloalkane
  • Alkyl halide (correct)
  • Organohalide
  • Alkyl fluoride
  • What is the key substituent in alkyl halide nomenclature?

    <p>The halide group</p> Signup and view all the answers

    Why are Greek letters often used in alkyl halide structure?

    <p>To label the carbons of the alkyl group attached to the halide</p> Signup and view all the answers

    What is the reason for labeling the carbons of the alkyl group attached to the halide?

    <p>The amount of branching at the alpha carbon affects the reaction mechanism</p> Signup and view all the answers

    What is the name of the commonly used organic solvent mentioned in the text?

    <p>Methylene chloride</p> Signup and view all the answers

    How many types of alkyl halides are mentioned in the text?

    <p>Three</p> Signup and view all the answers

    What is the main difference between saturated and unsaturated hydrocarbons?

    <p>The presence of single or multiple bonds between carbon atoms</p> Signup and view all the answers

    What is the general molecular formula for alkanes?

    <p>CnH2n+2</p> Signup and view all the answers

    What is the name of the simplest alkane?

    <p>Methane</p> Signup and view all the answers

    What is the classification of hydrocarbons that include alkanes, alkenes, and alkynes?

    <p>Aliphatic hydrocarbons</p> Signup and view all the answers

    What is the term for the process of naming organic molecules?

    <p>Nomenclature</p> Signup and view all the answers

    What is the main focus of the lesson?

    <p>Reactionary ability of both saturated and unsaturated hydrocarbons</p> Signup and view all the answers

    What is the main objective of this lecture?

    <p>To introduce the concepts of structure and nomenclature in organic chemistry</p> Signup and view all the answers

    What is the scope of the skill learned in this lecture?

    <p>Giving IUPAC names of unbranched alkanes/alkenes/alkynes having up to 20 carbon atoms</p> Signup and view all the answers

    What is the definition of organic chemistry?

    <p>The study of carbon-based compounds and their properties</p> Signup and view all the answers

    What are the three hydrocarbon families mentioned in the lecture?

    <p>Alkanes, alkenes, and alkynes</p> Signup and view all the answers

    Study Notes

    Leaving Groups

    • A good leaving group creates a partial charge on the site of attack to attract the negative charge of the nucleophile.
    • A leaving group must be able to stabilize the electrons it leaves with.

    Substitution Reactions

    • Examples of good leaving groups include those that create a positive charge to attract the nucleophile and can stabilize the electrons they leave with.

    Alkyl Halides

    • Alkyl halides are compounds where a carbon group (alkyl) is bonded to a halide (F, Cl, Br, or I).
    • The halide group is the key substituent in naming alkyl halides.

    Alkyl Halide Nomenclature

    • The steps to name a molecule include:
      • Identifying and naming the parent chain
      • Identifying the name of the substituents
      • Assigning a locant (number) to each substituent
      • Assembling the name alphabetically

    Alkyl Halide Structure

    • Greek letters are often used to label the carbons of the alkyl group attached to the halide.
    • Substitutions occur at the alpha carbon because the amount of branching at the alpha carbon affects the reaction mechanism.
    • There are three types of alkyl halides.

    Organic Chemistry

    • The study of carbon-based compounds and their properties.

    Hydrocarbons

    • Compounds that contain only C and H.
    • Divided into two main classes: aliphatic hydrocarbons and aromatic hydrocarbons.
    • Aliphatic hydrocarbons include: alkanes, alkenes, and alkynes.

    Aliphatic Hydrocarbons

    • Alkanes: have all the carbon atoms linked to each other by single electron-pair bonds (δ bonds).
    • Alkenes: contain one or more c-c double bonds (d.b).
    • Alkynes: contain one or more c-c triple bonds (t.b).

    Alkanes

    • Have general molecular formula CnH2n+2 where n is an integer.
    • The simplest one is methane (CH4).
    • Nomenclature: IUPAC names are used to identify unbranched alkanes having up to 20 carbon atoms.

    Cycloalkanes

    • Contain a closed ring of carbon atoms.

    Unsaturated Hydrocarbons

    • Alkenes: contain one or more c-c double bonds (d.b).
    • Alkynes: contain one or more c-c triple bonds (t.b).

    Aromatic Hydrocarbons

    • Also known as arenes.
    • Have properties that are much different from aliphatic hydrocarbons.
    • The most important aromatic hydrocarbon is benzene.

    Reactivity of Hydrocarbons

    • Functional groups in hydrocarbons determine their reactivity.
    • Reactionary ability of saturated hydrocarbons (alkanes, cycloalkanes) and unsaturated hydrocarbons (alkenes, alkadienes, alkynes).

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    Description

    Identify good leaving groups in substitution reactions, considering the two key criteria: creation of a partial charge and ability to stabilize electrons.

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