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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    a Diels-Alder reaction. Alkenes add to dienes to give cyclohexenes. This conversion is an example of a Diels-Alder reaction. Such reaction proceed with retention of stereochemistry. The rates are sensitive to electron-withdrawing or electron-donating substituents. When irradiated by UV-light, alkenes dimerize to give cyclobutanes. [20]

  3. Doering–LaFlamme allene synthesis - Wikipedia

    en.wikipedia.org/wiki/Doering–LaFlamme_allene...

    The reaction is a two-stage process, in which first the alkene is reacted with dichlorocarbene or dibromocarbene to form a dihalocyclopropane. This intermediate is then reacted with a reducing metal, such as sodium or magnesium, or with an organolithium reagent .

  4. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    Dehydrohalogenation to give an alkene In chemistry , dehydrohalogenation is an elimination reaction which removes a hydrogen halide from a substrate . The reaction is usually associated with the synthesis of alkenes , but it has wider applications.

  5. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    Usually the substrate is an alkene and the product is a nitrile. The reaction proceeds via the oxidative addition of HCN to a low-valent metal complex to give a hydrido cyanide complex. Subsequent binding of the alkene gives the intermediate M(H)(CN)L n (alkene), which then undergoes migratory insertion to give an alkylmetal

  6. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    A hydrohalogenation reaction is the electrophilic addition of hydrogen halides like hydrogen chloride or hydrogen bromide to alkenes to yield the corresponding haloalkanes. [ 1 ] [ 2 ] [ 3 ] If the two carbon atoms at the double bond are linked to a different number of hydrogen atoms, the halogen is found preferentially at the carbon with fewer ...

  7. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  8. Today’s NYT ‘Strands’ Hints, Spangram and Answers for ...

    www.aol.com/today-nyt-strands-hints-spangram...

    An example spangram with corresponding theme words: PEAR, FRUIT, BANANA, APPLE, etc. ... NYT Strands Spangram Answer Today. Today's spangram answer on Saturday, January 11, 2025, is TIMING.

  9. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    Cyclization reactions, or intramolecular addition reactions, can be used to form cycloalkenes. These reactions primarily form cyclopentenones, a cycloalkene that contains two functional groups: the cyclopentene and a ketone group. [12] However, other cycloalkenes, such as Cyclooctatetraene, can be formed as a result of this reaction. [11]