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  2. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–nitrogen_bond

    A CN bond is strongly polarized towards nitrogen (the electronegativities of C and N are 2.55 and 3.04, respectively) and subsequently molecular dipole moments can be high: cyanamide 4.27 D, diazomethane 1.5 D, methyl azide 2.17, pyridine 2.19. For this reason many compounds containing CN bonds are water-soluble.

  3. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    The bimolecular nucleophilic substitution (S N 2) is a type of reaction mechanism that is common in organic chemistry. In the S N 2 reaction, a strong nucleophile forms a new bond to an sp 3-hybridised carbon atom via a backside attack, all while the leaving group detaches from the reaction center in a concerted (i.e. simultaneous) fashion.

  4. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The two main mechanisms were the S N 1 reaction and the S N 2 reaction, where S stands for substitution, N stands for nucleophilic, and the number represents the kinetic order of the reaction. [ 4 ] In the S N 2 reaction, the addition of the nucleophile and the elimination of leaving group take place simultaneously (i.e. a concerted reaction ).

  5. Electrophilic amination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_amination

    A nitrogen bound to both a good electrofuge and a good nucleofuge is known as a nitrenoid (for its resemblance to a nitrene). [2] Nitrenes lack a full octet of electrons are thus highly electrophilic; nitrenoids exhibit analogous behavior and are often good substrates for electrophilic amination reactions.

  6. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    While nucleophilic acyl substitution reactions can be base-catalyzed, the reaction will not occur if the leaving group is a stronger base than the nucleophile (i.e. the leaving group must have a higher pK a than the nucleophile). Unlike acid-catalyzed processes, both the nucleophile and the leaving group exist as anions under basic conditions.

  7. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    Others, however, insist that such a usage is an abuse of terminology, and limit the Michael addition to the formation of carbon–carbon bonds through the addition of carbon nucleophiles. The terms oxa-Michael reaction and aza-Michael reaction [2] have been used to refer to the 1,4-addition of oxygen and nitrogen nucleophiles, respectively. The ...

  8. Jordan Chiles Makes Sexy “Sports Illustrated Swimsuit” Debut ...

    www.aol.com/jordan-chiles-makes-sexy-sports...

    The 2025 Sports Illustrated Swimsuit roster is growing.. On Monday, Nov. 11, the magazine announced that Olympic gymnast Jordan Chiles and pro surfer Caroline Marks would be featured in this year ...

  9. Tetrahedral carbonyl addition compound - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_carbonyl...

    Similarly, an interaction of an oxygen lone pair with σ* C-C orbital should be responsible for the lengthened C1-C2 bond [152.75(15) pm] compared to the average C sp2-C sp2 bonds which are 151.3 pm. Also, the C1-C11 bond [152.16(17) pm] is slightly shorter than the average C sp3-C sp3 bond which is around 153.0 pm. Carbinol tetrahedral ...