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Related Concept Videos

Factors Affecting α-Alkylation of Ketones: Choice of Base01:10

Factors Affecting α-Alkylation of Ketones: Choice of Base

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α-Alkylation of ketones is achieved in the presence of alkyl halides and a base. The reaction proceeds via the formation of an enolate ion followed by nucleophilic substitution. The choice of base employed is essential as it is the key factor in determining the reaction outcome.
The reaction involving bases like EtO− whose conjugate acid EtOH (pKa = 15.9) is stronger than the ketone (pKa = 19.2) results in an equilibrium mixture with higher ketone concentration. As a consequence,...
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Alkyl Halides02:45

Alkyl Halides

20.1K
Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
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Cellulose and Pectic Polysaccharides01:15

Cellulose and Pectic Polysaccharides

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 Every plant cell has a cell wall that protects the cell, provides structural support, and gives the cell shape. Cellulose, the main structural component of the plant cell wall, makes up over 30% of plant matter. It is the most abundant organic compound on earth.  Cellulose is an unbranched polysaccharide composed of linear chains of glucose molecules linked by β (1→4) glycosidic bonds.
As a cell matures, its cell wall specializes according to its type. For example, the...
5.0K
Preparation of Alkynes: Alkylation Reaction02:27

Preparation of Alkynes: Alkylation Reaction

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Introduction
Alkylation of terminal alkynes with primary alkyl halides in the presence of a strong base like sodium amide is one of the common methods for the synthesis of longer carbon-chain alkynes. For example, treatment of 1-propyne with sodium amide followed by reaction with ethyl bromide yields 2-pentyne.
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Mass Spectrometry: Alkyl Halide Fragmentation01:22

Mass Spectrometry: Alkyl Halide Fragmentation

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Chlorine isotopes exist as 35Cl and 37Cl in a 3:1 ratio, while bromine isotopes exist as 79Br and 81Br in a 1:1 ratio. The mass spectrum of alkyl halides typically produces two distinct molecular ion peaks, the molecular ion peak, [M], and the molecular ion plus two, [M + 2] peak. The relative heights of these two peaks are proportional to the isotopic abundance ratios of the halide. For example, 2‐chloropropane and 1‐bromopropane display two peaks with relative peak heights in a 3:1 and...
1.6K
Conversion of Alcohols to Alkyl Halides02:48

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8.5K
This lesson delves into the conversion of alcohols to corresponding alkyl halides and the mechanism of action for different reagents. Typically, the hydroxyl group is first protonated to convert it to a stable leaving group. Consequently, based on the starting alcohol, the mechanism undergoes either of the nucleophilic substitution routes, SN1 or SN2. Tertiary alkyl halides are made using the two-step SN1 mechanism that occurs via a carbocation intermediate, which is stabilized by...
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Studying Copper Nanoparticle-Induced Programmed Cell Death in Bacteria
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Tapioca Cellulose Based Copper Nanoparticles for Chemoselective N-Alkylation.

Md Shaharul Islam, Bablu Hira Mandal, Tapan Kumar Biswas

    Journal of Nanoscience and Nanotechnology
    |April 10, 2018
    PubMed
    Summary

    Researchers developed cellulose-supported poly(hydroxamic acid) copper nanoparticles from tapioca root. This novel bio-heterogeneous catalyst efficiently catalyzes N-alkylation reactions with high yields and excellent reusability.

    Keywords:
    N-AlkylationTapioca CellulosePoly(methyl acrylate)Poly(hydroxamic acid)Copper Nanoparticlesαβ-Unsaturated Compounds

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    Area of Science:

    • Materials Science
    • Catalysis
    • Green Chemistry

    Background:

    • Biomaterials are crucial supports for heterogeneous catalysts.
    • Tapioca root offers an abundant source for biopolymer synthesis.

    Purpose of the Study:

    • To synthesize and characterize cellulose-supported poly(hydroxamic acid) copper nanoparticles (CuN@PHA) using tapioca root.
    • To evaluate the catalytic efficiency of CuN@PHA in N-alkylation reactions.

    Main Methods:

    • Synthesis of cellulose-supported CuN@PHA from tapioca biopolymer.
    • Characterization using FTIR, UV-Vis, FESEM, XPS, ICP-AES, and TEM.
    • Catalytic testing of N-alkylation of aliphatic amines with α,β-unsaturated compounds.

    Main Results:

    • Successful synthesis and characterization of CuN@PHA.
    • High catalytic activity in N-alkylation, achieving yields up to 95%.
    • Excellent reusability of the catalyst over multiple cycles with sustained activity.

    Conclusions:

    • Tapioca-derived cellulose is an effective support for poly(hydroxamic acid) copper nanoparticles.
    • The CuN@PHA catalyst demonstrates high efficiency, stability, and reusability for N-alkylation.
    • This study highlights a sustainable approach to heterogeneous catalysis using abundant biomaterials.