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Τι (ποιος) είναι asymmetric chromosome rearrangement - ορισμός

Reilly–Hickinbottom rearrangement; Hofmann-Martius rearrangement; Reilly-Hickinbottom rearrangement

Asymmetric warfare

WAR BETWEEN BELLIGERENTS WHOSE RELATIVE MILITARY POWER DIFFERS SIGNIFICANTLY

Asymmetrical warfare; Asymmetric war; Asymmetric attack; Aysmmetric warfare; Asymmetric engagement; Asymetric warfare; Assymetric warfare; Asynchronous warfare; Asymetrical warfare; Assymetrical warfare; Asymmetric conflicts; Asymmetric conflict; Asymmetrical war; Asymmetrical conflict; Asymmetrical fighting; Symmetric warfare; Asymmetric Warfare

Asymmetric warfare (or asymmetric engagement) is the term given to describe a type of war between belligerents whose relative military power differs significantly, or whose strategy or tactics differ significantly. This is typically a war between a standing, professional army and an insurgency or resistance movement militias who often have status of unlawful combatants.

https://en.wikipedia.org/wiki/Asymmetric_warfare

Chromosomal rearrangement

In genetics, a chromosomal rearrangement is a mutation that is a type of chromosome abnormality involving a change in the structure of the native chromosome.UniProt.

https://en.wikipedia.org/wiki/Chromosomal_rearrangement

Pinacol rearrangement

REARRANGEMENT OF A 1,2-DIOL COMPOUND TO CARBONYL COMPOUND

Pinacol–pinacolone rearrangement; Pinacol-pinacolone rearrangement; Pinnacol–pinnacolone rearrangement; Pinnacol-pinnacolone rearrangement

The pinacol–pinacolone rearrangement is a method for converting a 1,2-diol to a carbonyl compound in organic chemistry. The 1,2-rearrangement takes place under acidic conditions.

https://en.wikipedia.org/wiki/Pinacol_rearrangement

Βικιπαίδεια

Hofmann–Martius rearrangement

The Hofmann–Martius rearrangement in organic chemistry is a rearrangement reaction converting an N-alkylated aniline to the corresponding ortho and / or para aryl-alkylated aniline. The reaction requires heat, and the catalyst is an acid like hydrochloric acid.

When the catalyst is a metal halide the reaction is also called the Reilly–Hickinbottom rearrangement.

The reaction is also known to work for aryl ethers and two conceptually related reactions are the Fries rearrangement and the Fischer–Hepp rearrangement. Its reaction mechanism centers around dissociation of the reactant with the positively charged organic residue R attacking the aniline ring in a Friedel–Crafts alkylation.

In one study this rearrangement was applied to a 3-N(CH₃)(C₆H₅)-2-oxindole:

The reaction is named after German chemists August Wilhelm von Hofmann and Carl Alexander von Martius.

https://en.wikipedia.org/wiki/Hofmann–Martius rearrangement