Scribd Logo
Upload

Welcome to Scribd!

  • 8K views

    Upload

    Uploaded by

    Wee Chin David Chin
    1. The combustion of cyclohexene in excess air will produce carbon dioxide and water. Combustion of cyclohexene is more sooty than cyclohexane because cyclohexene has a higher percentage of carbon by mass. 2. Bromine in diethyl ether reacts with cyclohexene to produce 1,2-dibromocyclohexane in a halogenation reaction. This reaction involves the addition of bromine to the carbon atom with the double bond. The reaction can occur spontaneously in both dark and light conditions because cyclohexene contains a double bond that bromine can add to.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOCX, PDF, TXT or read online from Scribd

    Upload

    Uploaded by

    Wee Chin David Chin
    8K views1 page
    1. The combustion of cyclohexene in excess air will produce carbon dioxide and water. Combustion of cyclohexene is more sooty than cyclohexane because cyclohexene has a higher percentage of carbon by mass. 2. Bromine in diethyl ether reacts with cyclohexene to produce 1,2-dibromocyclohexane in a halogenation reaction. This reaction involves the addition of bromine to the carbon atom with the double bond. The reaction can occur spontaneously in both dark and light conditions because cyclohexene contains a double bond that bromine can add to.

    Copyright

    © Attribution Non-Commercial (BY-NC)

    Available Formats

    DOCX, PDF, TXT or read online from Scribd

    Did you find this document useful?

    Is this content inappropriate?

    1. The combustion of cyclohexene in excess air will produce carbon dioxide and water. Combustion of cyclohexene is more sooty than cyclohexane because cyclohexene has a higher percentage of carbon by mass. 2. Bromine in diethyl ether reacts with cyclohexene to produce 1,2-dibromocyclohexane in a halogenation reaction. This reaction involves the addition of bromine to the carbon atom with the double bond. The reaction can occur spontaneously in both dark and light conditions because cyclohexene contains a double bond that bromine can add to.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    8K views1 page

    Upload

    Uploaded by

    Wee Chin David Chin
    1. The combustion of cyclohexene in excess air will produce carbon dioxide and water. Combustion of cyclohexene is more sooty than cyclohexane because cyclohexene has a higher percentage of carbon by mass. 2. Bromine in diethyl ether reacts with cyclohexene to produce 1,2-dibromocyclohexane in a halogenation reaction. This reaction involves the addition of bromine to the carbon atom with the double bond. The reaction can occur spontaneously in both dark and light conditions because cyclohexene contains a double bond that bromine can add to.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    of 1

    Discussions: 1. Discuss part A, B, C, D and E.

    In part A, the combustion of cyclohexene in excess air will produce carbon dioxide and water. Combustion of cyclohexene is more sooty compared to combustion of cyclohexane is because the percentage of carbon by mass in cyclohexene is higher compared to cyclohexane.

    In part B, the bromine in diethyl ether reacts with cyclohexene to produce 1,2dibromocyclohexane. This reaction is known as halogenations which involved the addition of halogen, bromine in this case, to the carbon atom with the double bond (C=C). In both dark and light surrounding, the reaction of bromine in diethyl ether with cyclohexene can be occurred spontaneously is because the cyclohexene molecules contain a double bond between two carbon atoms. In this case, cyclohexene behave as nucleophiles (Lewis base) in polar reaction, donating a pair of electrons from their electron-rich C=C bond to bromine which is the electrophile.

    You might also like

    pFad - Phonifier reborn

    Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

    Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


    Alternative Proxies:

    Alternative Proxy

    pFad Proxy

    pFad v3 Proxy

    pFad v4 Proxy