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ansomer

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The answer ANSOMER has 0 possible clue(s) in existing crosswords.

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There are 7 letters in ANSOMER ( A1E1M3N1O1R1S1 )

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Scrabble results that can be created with an extra letter added to ANSOMER

ALMONERS AMARONES TONEARMS SONARMEN ROMANCES ROMAINES RHAMNOSE RANSOMER RANSOMED OVERMANS ONSTREAM ROMANISE NEUROMAS MADRONES MORAINES ENAMOURS HORSEMAN FORAMENS MANROPES MENORAHS MONERANS MONSTERA

7 letters out of ANSOMER

ENAMORS MOANERS OARSMEN

6 letters out of ANSOMER

ARSENO ENAMOR MANORS MOANER NAMERS RAMOSE RAMSON RANSOM REASON REMANS ROMANS SENORA SERMON

5 letters out of ANSOMER

AEONS AMENS AROSE ARSON EARNS ENORM MANES MANOR MANOS MANSE MARES MARSE MASER MASON MEANS MENSA MESON MOANS MONAS MORAE MORAS MORES MORNS MORSE NAMER NAMES NARES NEARS NEMAS NOMAS NOMES NORMS OMENS OMERS RAMEN REAMS REMAN ROAMS ROANS ROMAN SANER SENOR SMEAR SNARE SNORE SOMAN SONAR

4 letters out of ANSOMER

AEON AERO AMEN ANES ARES ARMS ARSE EARN EARS EONS ERAS ERNS EROS MAES MANE MANO MANS MARE MARS MEAN MENO MESA MOAN MOAS MONS MORA MORE MORN MORS NAME NAOS NEAR NEMA NOES NOMA NOME NOMS NORM NOSE OARS OMEN OMER ONES ORES OSAR RAMS RASE REAM REMS ROAM ROAN ROES ROMS ROSE SAME SANE SEAM SEAR SERA SOAR SOMA SOME SONE SORA SORE SORN

3 letters out of ANSOMER

ANE ARE ARM ARS EAR EMS ENS EON ERA ERN ERS MAE MAN MAR MAS MEN MOA MON MOR MOS NAE NAM NOM NOR NOS OAR OES OMS ONE ONS ORA ORE ORS OSE RAM RAN RAS REM RES ROE ROM SAE SEA SEN SER SOM SON

2 letters out of ANSOMER

AE AM AN AR AS EM EN ER ES MA ME MO NA NE NO OE OM ON OR OS RE SO

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Ansomer might refer to
In organic chemistry, the Anomeric effect or Edward-Lemieux effect is a stereoelectronic effect that describes the tendency of heteroatomic substituents adjacent to a heteroatom within a cyclohexane ring to prefer the axial orientation instead of the less hindered equatorial orientation that would be expected from steric considerations. This effect was originally observed in pyranose rings by J. T. Edward in 1955 when studying carbohydrate chemistry.
* The term "anomeric effect" was introduced in 1958. The name comes from the term used to designate the lowest-numbered ring carbon of a pyranose (C1 in aldopyranoses, CN in ketopyranoses), the anomeric carbon. Isomers that differ only in the configuration at the anomeric carbon are called anomers. The anomers of D-glucopyranose are diastereomers, with the beta anomer having an OH group pointing up equatorially, and the alpha anomer having that OH group pointing down axially.
* The anomeric effect can also be generalized to any cyclohexyl or linear system with the general formula C-Y-C-X, where Y is a heteroatom with one or more lone pairs, and X is an electronegative atom or group. The magnitude of the anomeric effect is estimated at about 1–2 kcal/mol in the case of sugars, but is different for every molecule.* In the above case, the methoxy group on the cyclohexane ring (top) prefers the equatorial position. However, in the tetrahydropyran ring (bottom), the methoxy group prefers the axial position. This is because in the cyclohexane ring, Y= carbon, which is not a heteroatom, so the anomeric effect is not observed and sterics dominates the observed substituent position. In the tetrahydropyran ring, Y= oxygen, which is a heteroatom, so the anomeric effect contributes and stabilizes the observed substituent position. In both cases, X= OMe.
* The anomeric effect is most often observed when Y= oxygen, but can also be seen with other lone pair bearing heteroatoms in the ring, such as nitrogen, sulfur, and phosphorus.
* The exact method by which the anomeric effect causes stabilization is a point of controversy, and several hypotheses have been proposed to explain it.
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