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  2. Epimer - Wikipedia

    en.wikipedia.org/wiki/Epimer

    In stereochemistry, an epimer is one of a pair of diastereomers. [1] The two epimers have opposite configuration at only one stereogenic center out of at least two. [2] All other stereogenic centers in the molecules are the same in each. Epimerization is the interconversion of one epimer to the other epimer.

  3. Mutarotation - Wikipedia

    en.wikipedia.org/wiki/Mutarotation

    The rotation of the solution will increase from +18.7° to an equilibrium value of +52.7° as some of the β form is converted to the α form. The equilibrium mixture is about 64% of β- D -glucopyranose and about 36% of α- D -glucopyranose, though there are also traces of the other forms including furanoses and open chained form.

  4. Stereochemistry - Wikipedia

    en.wikipedia.org/wiki/Stereochemistry

    Stereochemistry, a subdiscipline of chemistry, studies the spatial arrangement of atoms that form the structure of molecules and their manipulation. [1] The study of stereochemistry focuses on the relationships between stereoisomers, which are defined as having the same molecular formula and sequence of bonded atoms (constitution) but differing in the geometric positioning of the atoms in space.

  5. Stereocenter - Wikipedia

    en.wikipedia.org/wiki/Stereocenter

    In stereochemistry, a stereocenter of a molecule is an atom (center), axis or plane that is the focus of stereoisomerism; that is, when having at least three different groups bound to the stereocenter, interchanging any two different groups creates a new stereoisomer. [1] [2] Stereocenters are also referred to as stereogenic centers.

  6. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    If the two substituents on at least one end of a double bond are the same, then there is no stereoisomer and the double bond is not a stereocenter, e.g. propene, CH 3 CH=CH 2 where the two substituents at one end are both H. [6] Traditionally, double bond stereochemistry was described as either cis (Latin, on this side) or trans (Latin, across ...

  7. The new college student sex trend and why it's so dangerous

    www.aol.com/college-student-sex-trend-why...

    A new sex trend among college students is getting attention on TikTok − and it has doctors worried.. That trend is using honey packets, a controversial supplement marketed for sexual enhancement ...

  8. 17 Easy & Cozy Breakfasts for Winter - AOL

    www.aol.com/17-easy-cozy-breakfasts-winter...

    December 3, 2024 at 6:15 PM. Joy Howard. ... For those mornings when choosing between red or green salsa feels impossible, enter huevos divorciados, the ultimate solution. It features two sunny ...

  9. Diastereomer - Wikipedia

    en.wikipedia.org/wiki/Diastereomer

    In stereochemistry, diastereomers (sometimes called diastereoisomers) are a type of stereoisomer. [1] Diastereomers are defined as non-mirror image, non-identical stereoisomers. Hence, they occur when two or more stereoisomers of a compound have different configurations at one or more (but not all) of the equivalent (related) stereocenters and ...