rearrangement

(redirected from Rearrangement reaction)
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Related to Rearrangement reaction: addition reaction, Beckmann rearrangement, Pericyclic reaction

re·ar·range

 (rē′ə-rānj′)
tr.v. re·ar·ranged, re·ar·rang·ing, re·ar·rang·es
To change the arrangement of.

re′ar·range′ment n.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.rearrangement - changing an arrangement
juggle, juggling - the act of rearranging things to give a misleading impression
musical chairs - a rearrangement that has no practical effect or significance; "the company is looking for stability after years of musical chairs with directors"; "shareholders don't want the company playing musical chairs with their investment"
reordering - a rearrangement in a different order
transposition - (electricity) a rearrangement of the relative positions of power lines in order to minimize the effects of mutual capacitance and inductance; "he wrote a textbook on the electrical effects of transposition"
arranging, transcription, arrangement - the act of arranging and adapting a piece of music

rearrangement

noun
A change in normal place or position:
Translations
إعادَة تَرْتيب
přeřazenípřeskupení
omrokering
átrendezés
endurskipulagning
preskupenie
yeniden düzenleme

rearrangement

[ˈriːəˈreɪndʒmənt] N [of meeting] → cambio m de fecha/hora; [of furniture] (= act) → cambio m de sitio; (= effect) → nueva disposición f

rearrangement

n (of furniture, system)Umstellung f; (of plans, layout, formation, order, ideas)Änderung f; (of appointment, meeting)Neuabmachung f

rearrangement

[ˌriːəˈreɪndʒmnt] n (see vt) → ridisposizione f, cambiamento

rearrange

(riːəˈreindʒ) verb
to change the position of; to arrange differently. We'll rearrange the chairs.
ˌreaˈrrangement noun
References in periodicals archive ?
As you can observe, stereoisomer rearrangement reaction rate is very low and not a significant concern with reactions rates being on the order of R22 reduction reaction stability and well below R11, R12 and R123 reduction reactions.
These results indicated that substituents at 2-position are critical for this rearrangement reaction. And the various groups at 1,2-positions had slight effect on the denitrosylation.
5) of the F.I., it was pointed out from the early stages of its discovery that the first cyclization step resembles the Claisen rearrangement reaction, which is known as a typical sigmatropy reaction.