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2. webbook.nist.gov › cgi › cbookN-Phenylcyclohexylamine - NIST Chemistry WebBook

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   Feb 6, 2010 · N-Phenylcyclohexylamine. Formula: C 12 H 17 N. Molecular weight: 175.2701. IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11 (8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2. Copy Sheet of paper on top of another sheet. IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N.

3. www.ocr.org.uk › Images › 359182-organic-synthesisSynthetic routes (A Level) reaction pathways Aliphatic compounds

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   OCR, A Level, Chemistry A, Topic Exploration Pack, Reaction pathways Created Date: 20170207082346Z ...

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4. People also ask

   Which reaction pathways are used in phenols dilute HNO3 Br 2 NaOH(aq)?

   • Version 1 © OCR 2017 Synthetic routes (A Level) reaction pathways - Phenols dilute HNO3 Br 2 NaOH(aq) and Version 1 © OCR 2017 Haloalkane Nitrile Amine Alkene Aldehyde Ketone Carboxylic acid Acyl chloride Ester Carboxylate Alkane Hydroxynitrile Synthetic routes (A Level) reaction pathways - Aliphatic compounds Alcohol 1°

   Synthetic routes (A Level) reaction pathways Aliphatic compounds

   www.ocr.org.uk/Images/359182-organic-synthesis-reaction-pathways.pdf

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   What are synthetic routes (a level) reaction pathways?

   • Synthetic routes (A Level) reaction pathways - Aromatic compounds Version 1 © OCR 2017 Synthetic routes (A Level) reaction pathways - Phenols dilute HNO3 Br 2 NaOH(aq) and Version 1 © OCR 2017 Haloalkane Nitrile Amine Alkene Aldehyde Ketone Carboxylic acid Acyl chloride Ester Carboxylate Alkane Hydroxynitrile

   Synthetic routes (A Level) reaction pathways Aliphatic compounds

   www.ocr.org.uk/Images/359182-organic-synthesis-reaction-pathways.pdf

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   How are arylamines prepared?

   • Arylamines are typically prepared by the reduction of a nitro group on an aromatic ring. Several methods for reducing nitro groups to amines are known. These include catalytic hydrogenation (H 2 + platinum catalyst), and zinc, iron, or tin (II) chloride in dilute mineral acid. The procedures described above are sufficient for most cases.

   24.6: Synthesis of Amines - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/24:_Amines_and_Heterocycles/24.06:_Synthesis_of_Amines

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   Which pathway provides the simplest amine starting material?

   • Because the amine is commonly used in excess during a reductive animation, the pathway which provides the simplest amine starting material is preferred. The carbon from the broken C-N bond goes on to become a carbonyl starting material. The nitrogen gains a hydrogen to become the amine starting material.

   24.6: Synthesis of Amines - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/24:_Amines_and_Heterocycles/24.06:_Synthesis_of_Amines

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5. chem.libretexts.org › Bookshelves › Organic_Chemistry24.6: Synthesis of Amines - Chemistry LibreTexts

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   If more than one pathway is possible, draw them both and determine which one would be preferred. Answer. Pathway 1. Solution 1. Pathway 2. Solution 2. Because N-methylbenzylamine has two C-N bonds there are two possible synthesis pathways. Pathway 1 is most likely preferred because it uses the simplest amine starting material, methyl amine.

6. pubchem.ncbi.nlm.nih.gov › 1-phenylcyclohexylamine1-Phenylcyclohexylamine | C12H17N | CID 31862 - PubChem

   pubchem.ncbi.nlm.nih.gov › 1-phenylcyclohexylamine

   Oct 14, 2021 · 1-Phenylcyclohexylamine | C12H17N | CID 31862 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

7. webbook.nist.gov › cgi › cbookN-Phenylcyclohexylamine - NIST Chemistry WebBook

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   For Zoom; 1.) Enter the desired X axis range (e.g., 100, 200) 2.) Check here for automatic Y scaling 3.) Press here to zoom

   • Date: 1959/09/22
   • Origin: MONSANTO (J. FREEMAN)

   • Name(s): N-cyclohexylanilineN-cyclohexyl-N-phenylamine
   • Source reference: COBLENTZ NO. 08474

8. www.masterorganicchemistry.com › 2018/11/19Synthesis (7): Reaction Map of Benzene and Related Aromatic ...

   www.masterorganicchemistry.com › 2018/11/19

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   Nov 19, 2018 · Reactions of Benzene and Aromatic Compounds: A Reaction Map (PDF) Let’s map out all of the reactions we’ve learned in this section on aromatic rings + substituents. The list comes to about 25, including. the six key electrophilic aromatic substitution reactions, the Wolff-Kishner and Clemmensen reductions of ketones.

9. chemrevise.org › wp-content › uploads3.14 Revision Guide Organic Synthesis AQA - chemrevise

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   Allow the layers to separate in the funnel, and then run and discard the aqueous layer. Run the organic layer into a clean, dry conical flask and add three spatula loads of drying agent (e.g. anhydrous sodium sulfate, calcium chloride) to dry the organic liquid. When dry the organic liquid should appear clear.