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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. Exercise \(\PageIndex{1}\)
OCR, A Level, Chemistry A, Topic Exploration Pack, Reaction pathways Created Date: 20170207082346Z ...
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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.
Revision notes on 7.8.2 Multi-step Synthetic Routes for the CIE A Level Chemistry syllabus, written by the Chemistry experts at Save My Exams.
2. Main activity: The pathway Discuss the fact that vanillin is an organic compound, so can be made from the organic compound benzene using a series of chemical reactions. Give each student a copy of page 2 of the student worksheet. They will now work alone, or in pairs, to complete question 2 part a on page 1.
Reaction 1—secondary aldehyde to ketone—is also an oxidation reaction. 4. UV light and Cl2 are both required. 5. Addition reaction. 6. HCl is the reagent required for both reactions 5 and 6. The products are different because the HCl has added across the double bond in a different orientation. In reaction 5, the Cl has added onto carbon 1 ...
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.
