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  2. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    A singlet carbene contains an empty p orbital and a roughly sp 2 hybrid orbital that has two electrons. Singlet carbenes add stereospecifically to alkenes, and alkene stereochemistry is retained in the cyclopropane product. [1] The mechanism for addition of a carbene to an alkene is a concerted [2+1] cycloaddition (see figure).

  3. Carbene - Wikipedia

    en.wikipedia.org/wiki/Carbene

    Carbene addition to alkenes. Singlet and triplet carbenes exhibit divergent reactivity. [11] [page needed] [12] Triplet carbenes are diradicals, and participate in stepwise radical additions. Triplet carbene addition necessarily involves (at least one) intermediate with two unpaired electrons.

  4. Cyclopropanation - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanation

    Cyclopropanation is also stereospecific as the addition of carbene and carbenoids to alkenes is a form of a cheletropic reaction, with the addition taking place in a syn manner. For example, dibromocarbene and cis-2-butene yield cis-2,3-dimethyl-1,1-dibromocyclopropane, whereas the trans isomer exclusively yields the trans cyclopropane. [16]

  5. Dichlorocarbene - Wikipedia

    en.wikipedia.org/wiki/Dichlorocarbene

    Dichlorocarbene reacts with alkenes in a formal [1+2]cycloaddition to form geminal dichlorocyclopropanes. These can be reduced to cyclopropanes or hydrolysed to give cyclopropanones by a geminal halide hydrolysis. Dichlorocyclopropanes may also be converted to allenes in the Skattebøl rearrangement.

  6. Cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Cycloaddition

    Strained alkenes like trans-cycloheptene derivatives have also been reported to react in an antarafacial manner in [2 + 2]-cycloaddition reactions. Doering (in a personal communication to Woodward ) reported that heptafulvalene and tetracyanoethylene can react in a suprafacial-antarafacial [14 + 2]-cycloaddition.

  7. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    Wyatt et al. have studied the regioselectivity of the thermal Buchner reaction using Rh 2 (O 2 CCF 3) 4 and demonstrated that the electrophilic character of the rhodium carbene prefers reaction at the more nucleophilic π-bonds of the aromatic ring. [15] regioselectivity. The accepted carbene catalytic cycle [16] was proposed by Yates [17] in ...

  8. Today's Wordle Hint, Answer for #1325 on Monday, February 3, 2025

    www.aol.com/todays-wordle-hint-answer-1325...

    SPOILERS BELOW—do not scroll any further if you don't want the answer revealed. The New York Times Today's Wordle Answer for #1325 on Monday, February 3, 2025

  9. Triazol-5-ylidene - Wikipedia

    en.wikipedia.org/wiki/Triazol-5-ylidene

    As opposed to the now ubiquitous NHC (N-heterocyclic carbene) systems based on imidazole rings, these carbenes are structured from triazole rings. 1,2,4-triazol-5-ylidene can be thought of as an analog member of the NHC family, with an extra nitrogen in the ring, while 1,2,3-triazol-5-ylidene is better thought of as a mesoionic carbene (MIC). [1]