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- are you able to identify an unknown stucture with the information you provided above and additionally: this compound is a solid, has a melting point <100 degrees celsius, tested negative for Jones oxidation and for Tollens test; and tested positive for Iodoform testGive the main organic product of the reaction in Figure 6. [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] * Your answerHello, I do not understand these questions for chemistry and I am stuck. May I get help please please?? Thank you. Synthesize the following compound starting with the alcohols shown. All carbons must come from molecules of the alcohols shown.
- WHich statement is true? Statement 1: When Sodium Detection for Active Hydrogen test was conducted with 2-butyne, hydrogen gas will be produced. Statement 2: When alkene is subjected to Baeyer's Test for Unsaturation, the formation of a brown suspension will be observed. This is due to the presence of MnO2 which is the reduction product of the confirmatory reagent KMnO4.Starting from a terminal alkene R-CH=CH2, is there any advantage in using the two-step protocol (halohydrin formation + intramolecular williamson) over the direct epoxidation procedure? HINT: check for other reactions of MCPBA. Is this also an oxidant for other funcional groups? WHich ones? would a chemoselectivity problem be expected if those functional groups were also present during the epoxidation reaction?NOTE : I POSTED THIS QUESTION PREVIOUSLY BUT THE WRONG ANSWER WAS PROVIDED. PLEASE POST RIGHT ANSWER. ALSO TWO PRODUCTS MUST BE FORMED. THANKS.
- Answer this connected questions. Upvote guaranteed. Don't forget to put iupac name on products.Make a table of the physical properties (molar mass, MPT, BPT density and mass used/needed) for the reduction of benzophenone lab reactions. (bezhydrol is the product of reaction). Plz do fast asap, urgent.Predict the MAJOR product for the following are new with nitric acid/acetic anhydride (reagents for EAS nitration) A. Benzaldehyde B. Cumene (isopropylbenzene) C. A mixture of A and B (which one is major and forms fastest)? Justify with sigma complex analysis show work and steps.
- Question 7: Write a mechanism for the nucleophilic addition reaction in Figure 7. Note that the reaction mixture does not contain an acid catalyst. How many elementary steps are there in the mechanism? Hint: Remember that water is polar like HCl. [The answer is a whole number.] * Your answer Question 9: The product of the reaction in Figure 7 is the main product of the reaction. Draw the structure of the by-product of the reaction. [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] * Your answerStep 1 Since you have asked multiple questions, we will solve the first question for you. If you want any specific question to be solved then please specify the question number or post only that question. 1. Sol :- Given incomplete reaction is : CH4 + Cl2, hv ------------> (a). Predict products and write complete chemical equation. (b) Write a stepwise mechanism for monochlorinated product formation. Be sure to show all the intermediate structure and all the electron flow using arrows. arrow_forward Step 2 (a). The given reaction is the photochlorination of methane, which undergoes free radical substitution mechanism in the presence of Cl2, light (hv) o gives mixture of products that is CH3Cl, CH2Cl2, CHCl3 and CCl4. In this reaction, one H of methane is replaced by Cl atom. Therefore, complete reaction is : arrow_forward Step 3 (b). Complete mechanism of photochlorination reaction is : Step.1 :- Chain initiation step :- Step.2 :- Chain propagation steps :-…help with (Oxidation of Cyclohexanol) post-lab questions. Explain in a paragraph, please. Why does the initial product (before the HCl addition) not precipitate from the solution?