You may want to reference (Pages 523-526) Section 11.5 while completing this problem. Draw the products of ring-closing metathesis for each of the following compounds. OCH₁ Draw the molecules on the canvas by choosing buttons from the Tools (for bonds). toolbars. The single bond is active by default. DCQQ H 100\ 3 IU ZO

You may want to reference (Pages 523-526) Section 11.5 while completing this problem. Draw the products of ring-closing metathesis for each of the following compounds. OCH₁ Draw the molecules on the canvas by choosing buttons from the Tools (for bonds). toolbars. The single bond is active by default. DCQQ H 100\ 3 IU ZO

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 7E: When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2)...

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You may want to reference (Pages 523-526) Section 11.5 while completing this problem. Draw the products of ring-closing metathesis for each of the following compounds. OCH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds). toolbars. The single bond is active by default. DCQQ H 0001 CONT H C N 0
When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?
Predict the products of this organic reaction: ? CH3-C-O-CH2-O-CH3 nghi KOH Specifically, in the drawing area below draw the structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Click anywhere to draw the first atom of your structure. C C X
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МЕСНANISMS 1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed opening of the epoxide ring to form two different products. > Using ethanol as the solvent and an appropriate acid, show the steps in the acid catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). > Using ethanol as the solvent and an appropriate base, show the steps in the base- catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). 1,2-epoxy-1-methylcyclopentane CH3
Provide the major organic product of the reaction shown. Na₂Cr₂O7, H₂SO4 'OH Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
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