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Related Concept Videos

Experimental Determination of Chemical Formula02:37

Experimental Determination of Chemical Formula

The elemental makeup of a compound defines its chemical identity, and chemical formulas are the most concise way of representing this elemental makeup. When a compound’s formula is unknown, measuring the mass of its constituent elements is often the first step in determining the formula experimentally.
Basicity of Heterocyclic Aromatic Amines01:25

Basicity of Heterocyclic Aromatic Amines

Heterocyclic amines, where the N atom is a part of an alicyclic system, are similar in basicity to alkylamines. Interestingly, the heterocyclic amine having a nitrogen atom as part of an aromatic ring has much less basicity than its corresponding alicyclic counterpart. For this reason, as presented in Figure 1, piperidine (pKb = 2.8) is significantly more basic than pyridine (pKb = 8.8).

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Updated: Jun 1, 2026

Color Spot Test As a Presumptive Tool for the Rapid Detection of Synthetic Cathinones
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Published on: February 5, 2018

6-Bromo-pyridine-2-carboxamide.

Feng Xue1, Shen-Gui Ju

  • 1College of Chemistry and Chemical Engineering, Nanjing University of Technology, Xinmofan Road No. 5 Nanjing, Nanjing 210009, People's Republic of China.

Acta Crystallographica. Section E, Structure Reports Online
|May 18, 2011
PubMed
Summary
This summary is machine-generated.

This study details the crystal structure of a brominated organic compound. It reveals intra-molecular hydrogen bonds forming a ring and inter-molecular bonds creating sheet-like structures in the solid state.

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Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
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Area of Science:

  • Crystal chemistry
  • Organic chemistry
  • Supramolecular chemistry

Background:

  • Understanding the hydrogen bonding patterns in organic molecules is crucial for predicting their solid-state properties.
  • The specific compound C(6)H(5)BrN(2)O presents an interesting case for crystallographic analysis due to its functional groups.

Purpose of the Study:

  • To elucidate the crystal structure of the title compound C(6)H(5)BrN(2)O.
  • To identify and characterize the hydrogen bonding interactions present in the crystal lattice.

Main Methods:

  • Single-crystal X-ray diffraction was employed to determine the molecular and crystal structure.
  • Analysis of the crystal structure focused on identifying hydrogen bond donors and acceptors.

Main Results:

  • An intra-molecular N-H⋯N hydrogen bond was observed, forming a stable S(5) ring motif.
  • Inter-molecular bifurcated N-H⋯(O,O) hydrogen bonds were identified, linking molecules into extended sheets.
  • The sheets propagate along the (100) direction in the crystal.

Conclusions:

  • The crystal packing of C(6)H(5)BrN(2)O is dominated by a combination of intra- and inter-molecular hydrogen bonding.
  • The observed hydrogen bonding network dictates the formation of sheet-like supramolecular architecture.