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- Can you help me number 8 part A ? Which is the formula of this rule of reaction (decarboxylation reaction)?Draw the intermediate product and the final product for the synthesis of ethyl 3-coumarin carboxylate.What have you learned so far? 1. Can you give an example of organic compounds or substances belonging to this family and its importance to us? 2. How can we name the carboxylic acids and its derivative? Give 1 example. 3. How does the nucleophilic acyl substitution undergo?
- Explain why pentane-2,4-dione forms two alkylation products (A and B) when the number ofequivalents of base is increased from one to two.Explain why pentane-2,4-dione forms two different alkylation products (Aor B) when the number of equivalents of base is increased from one totwo.Oa) An amine can be formed when 2-iodopentane is heated with ammonia in a sealed tube. This is an example of a nucleophilic substitution reaction. i) Provide a full equation (using condensed formula) for this reaction. You should name the reactants and the overall products as part of your response. ii) Name the organic product formed from this reaction and draw it's displayed structure. iii) Provide a 'curly arrow' mechanism (in displayed formula) with an accompanying explanation for this process. iv) Describe a characteristic test (with the result that would be observed) to show the presence of the amine produced upon completion of the nucleophilic substitution reaction. b) The amine produced in the above reaction forms a mixture of two optical isomers. i) Draw the 3D structures of the two isomers of the amine product that you named and produced a drawing of in part a ii). ii) With reference to a different named example, explain the term 'optical isomer'. You should draw the 3D…
- a)Step by step show the reaction of 1 mol of water from the 3,3-dimethyl-2-pentanol compound in acid-catalyzed medium.Name the main product formed. b)Indicate whether the resulting product shows the geometric isomer or not. c)Write the products formed when the product is ozonized and oxidized.If the Product of this Suzuki reaction is 4-(4-methylphenyl)benzaldehyde, what are the two starting reagents. Please write the name of the structures along with the drawing of the starting reagents.Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. Thank you for your help!
- Explain two different ways to introduce an alkyl group on a benzene ring ?20:32 hydroxide 2. Using curved arrows, show the deprotonation mechanism of phenol with (OH). Also, provide the structure of the product of this deprotonation. Start answering this question by drawing the structure of phenol. Then hydroxide ion. Find your most reactive electrons and draw the curved arrow that shows where they would go to deprotonate phenol. Then "make a bond break a bond" write they question 3. Provide valid resonance structures for the product of the previous arrow(s) charge moving onto the ortho- and para positions. Use curved to show how the charge resonates to the next structure in your scheme. all the proper notations for depicting resonance. that show the in the structures Be sure to use Send a chat CCarboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?