Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CH3 CH3 Br2 / FeBr3 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.
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- List the following carbocation intermediates in order from least stable to most stable. Explain why they were ranked this way.Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the intermediate and product in this reaction. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts.What is the intermediate of the reaction based on the image below?
- - For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structure of the major product of the elimination. (Picture 1): Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate. Note: HSO−4HSO4− is formed from step 1, but not shown. (Picture 2): Step 3: Use a curved arrow to show the carbocation rearrangement. Step 4: Draw curved arrows to show the elimination to form the major product. Water is added as a base. - Draw the major product of the elimination. H3O+H3O+ has been pre‑drawn for your convenience.Fill in the reagents below/above the arrow in the ff reactionCurved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the missing reactants/intermediates in this SN1 mechanism. Include all lone pairs. Ignore byproducts. Ignore stereochemistry.
- Match the conditions most favorable for the substitution reaction type (SN1 or SN2) Strong nucleophile Tertiary carbocation intermediate Protic solvent Primary carbocation intermediateDraw the products for the addition reactions below in the boxes. Then, draw the FULL electron-pushing mechanism for the reactions, including all intermediates (with formal charges and lone pairs of electrons) and all electron pushing arrows. Label the electrophile and nucleophile in each step.For 10.29, the trans product (major product) and the cis product (third product) are displayed as possible E2 products. However, for 10.30, only the trans product (major product) is shown. How come the cis product is not needed?
- Draw the structure of the major organic product(s) of the reaction. You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.what intermediate is formed in the reaction below?The SN1 reaction is a two-step reaction, and the first step of this reaction is the formation of a carbocation intermediate. Draw the carbocation intermediates that form from the alkyl chlorides in tubes 8 and 15. 2. Again, use tubes 8 and 15 to answer the following question. In general, the more stable carbocation forms faster. Given this, which carbocation is more stable, or do they have the same stability?