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Related Concept Videos

Precipitation Titration: Endpoint Detection Methods01:19

Precipitation Titration: Endpoint Detection Methods

In argentometric precipitation titrations, endpoints can be detected visually by the Mohr, Volhard, and Fajans methods. In the Mohr method, adding a soluble chromate indicator gives an initial yellow color to the analyte solution. As the titrant is added, the first excess of silver ions forms a red silver chromate precipitate, marking the endpoint. The solution pH should be maintained at about 8 by adding solid CaCO3.
In the Volhard method, a standard excess of AgNO3 is first added to the...
Qualitative Analysis03:46

Qualitative Analysis

For solutions containing mixtures of different cations, the identity of each cation can be determined by qualitative analysis. This technique involves a series of selective precipitations with different chemical reagents, each reaction producing a characteristic precipitate for a specific group of cations. Metal ions within a group are further separated by varying the pH, heating the mixture to redissolve a precipitate, or adding other reagents to form complex ions.
For instance, group IV...
Masking and Demasking Agents01:19

Masking and Demasking Agents

EDTA titrations may necessitate masking and demasking agents to temporarily protect a particular metal ion in a mixture from the EDTA reaction. These agents facilitate the sequential analysis of the metal ions by forming stable complexes with some—but not all—metal ions during certain steps.
There are many masking agents, such as cyanide, fluoride, triethanolamine, thiourea, and 2,3-bis(sulfanyl)propan-1-ol (formerly 2,3-dimercapto-1-propanol), with the masking agent chosen based on the metal...
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions01:20

Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions

Arenediazonium substitution reactions occur when the diazonium group is substituted by various functional groups such as halides, hydroxyl, nitrile, etc. For instance, arenediazonium salts react with copper(I) salts of chloride, bromide, or cyanide to form corresponding aryl chlorides, bromides, and nitriles. These reactions are named Sandmeyer reactions. Although the mechanism of this reaction is complicated, as illustrated in Figure 1, they are believed to progress via an aryl copper...

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Related Experiment Video

Updated: Jun 1, 2026

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
09:04

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products

Published on: September 9, 2016

Guanidinium chloro-chromate.

Hoong-Kun Fun, Jia Hao Goh, Arnab Kar

    Acta Crystallographica. Section E, Structure Reports Online
    |May 18, 2011
    PubMed
    Summary

    Crystallographic mirror symmetry was observed in guanidinium chloridotrioxidochromate(VI). This study details the crystal structure, revealing delocalization in the guanidinium cation and hydrogen bonding that forms infinite chains.

    Area of Science:

    • Inorganic Chemistry
    • Crystallography
    • Solid-State Chemistry

    Background:

    • Guanidinium salts are widely studied for their unique structural and chemical properties.
    • Chromium(VI) compounds exhibit diverse coordination chemistries and oxidation states.
    • Understanding crystal structures provides insights into bonding and intermolecular interactions.

    Purpose of the Study:

    • To elucidate the crystal structure of guanidinium chloridotrioxidochromate(VI).
    • To investigate the symmetry elements and bonding characteristics within the compound.
    • To analyze the intermolecular interactions and their role in crystal packing.

    Main Methods:

    • Single-crystal X-ray diffraction analysis.
    • Bond length and angle measurements.

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    Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
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    Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
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    Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides

    Published on: May 26, 2019

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    Last Updated: Jun 1, 2026

    A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
    09:04

    A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products

    Published on: September 9, 2016

    Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
    09:45

    Modification and Functionalization of the Guanidine Group by Tailor-made Precursors

    Published on: April 27, 2017

    Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
    07:50

    Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides

    Published on: May 26, 2019

  • Analysis of intermolecular hydrogen bonding and symmetry operations.
  • Main Results:

    • The guanidinium cation and chloridotrioxidochromate(VI) anion exhibit crystallographic mirror symmetry.
    • Intermediate C-N bond lengths in the guanidinium cation indicate significant electron delocalization.
    • Intermolecular N-H⋯Cl interactions form R(2)(1)(6) ring motifs, further linked by N-H⋯O hydrogen bonds into infinite chains along the [010] direction.

    Conclusions:

    • The crystal structure of guanidinium chloridotrioxidochromate(VI) is characterized by symmetry and extensive hydrogen bonding.
    • Delocalization within the guanidinium cation influences its structural parameters.
    • The observed hydrogen bonding network dictates the formation of extended chain structures in the solid state.