The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols

Detalhes bibliográficos
Autor(a) principal: Crespo,Lívia T. C.
Data de Publicação: 2013
Outros Autores: Mattos,Marcio C. S. de, Esteves,Pierre M.
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422013000200019
Resumo: Primary, secondary and tertiary alcohols can be easily distinguished due to their reactivity towards tribromoisocyanuric acid (TBCA). The test is performed by adding TBCA to the alcohol in a test tube heated in a boiling water bath. Orange color develops in the tube containing the primary alcohol, light yellow is observed in the tube containing the secondary alcohol while the tertiary alcohol results in a colorless mixture.
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spelling The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcoholstribromoisocyanuric acidalcoholsspot testPrimary, secondary and tertiary alcohols can be easily distinguished due to their reactivity towards tribromoisocyanuric acid (TBCA). The test is performed by adding TBCA to the alcohol in a test tube heated in a boiling water bath. Orange color develops in the tube containing the primary alcohol, light yellow is observed in the tube containing the secondary alcohol while the tertiary alcohol results in a colorless mixture.Sociedade Brasileira de Química2013-01-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422013000200019Química Nova v.36 n.2 2013reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422013000200019info:eu-repo/semantics/openAccessCrespo,Lívia T. C.Mattos,Marcio C. S. deEsteves,Pierre M.eng2013-03-18T00:00:00Zoai:scielo:S0100-40422013000200019Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2013-03-18T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
title The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
spellingShingle The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
Crespo,Lívia T. C.
tribromoisocyanuric acid
alcohols
spot test
title_short The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
title_full The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
title_fullStr The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
title_full_unstemmed The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
title_sort The use of tribromoisocyanuric acid to distinguish among primary, secondary and tertiary alcohols
author Crespo,Lívia T. C.
author_facet Crespo,Lívia T. C.
Mattos,Marcio C. S. de
Esteves,Pierre M.
author_role author
author2 Mattos,Marcio C. S. de
Esteves,Pierre M.
author2_role author
author
dc.contributor.author.fl_str_mv Crespo,Lívia T. C.
Mattos,Marcio C. S. de
Esteves,Pierre M.
dc.subject.por.fl_str_mv tribromoisocyanuric acid
alcohols
spot test
topic tribromoisocyanuric acid
alcohols
spot test
description Primary, secondary and tertiary alcohols can be easily distinguished due to their reactivity towards tribromoisocyanuric acid (TBCA). The test is performed by adding TBCA to the alcohol in a test tube heated in a boiling water bath. Orange color develops in the tube containing the primary alcohol, light yellow is observed in the tube containing the secondary alcohol while the tertiary alcohol results in a colorless mixture.
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422013000200019
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422013000200019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0100-40422013000200019
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Química Nova v.36 n.2 2013
reponame:Química Nova (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Química Nova (Online)
collection Química Nova (Online)
repository.name.fl_str_mv Química Nova (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv quimicanova@sbq.org.br
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