Below, depicts the electron flow process for the synthetic schemes. This should include theprediction of significant and by-products through electronic and structural impacts. The mechanismfor pushing the arrow must be shown.SYNTHESIS OF TEREPHTALIC ACIDAICI3CH3CI+ HCItolueneScheme 1. Formm of Yeluere wme 'rerke: Cra AlistarenBr2FeBr3Brtolueneo-Bromotoluenep-BromotolueneScheme 2. Bronination of Toluene using Bry/FeBrMgC=CBrMoBretherp-Bromotoluenephenylmagnesium bromideacetic acidScheme 3. Bromo I methyl bencene forms Grignard reagent upon reactingmagnesiumKMN04HOOHacetic acidTerephthalic acidScheme 4. Bronno i metlyl benzoie ccid undergo axicetion in presence of poassimpermangravate to form CXOH and we get the desired acad (Tereplthale ocid)

Answered: Image /qna-images/answer/bf28449b-5090-4efb-b46e-24fe4669114a.jpg

Answered: Below, depicts the electron flow…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 11E

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Given this organic synthesis, is there any limiting and excess reagents? also describe the procedure is run, how is the reaction monitored?Is the order fo addition important? N-ETHYLALLENIMINE[Aziridine, 1-ethyl-2-methylene-] Submitted by Albert T. Bottini and Robert E. Olsen1.Checked by Thomas H. Lowry and E. J. Corey. 1. ProcedureCaution! This preparation should be carried out in a good hood to avoid exposure to ammonia. The operator should wear rubber gloves and protective goggles because 2-haloallylamines and ethylenimines can cause severe skin and eye irritation. A 2-l. three-necked flask is fitted with a sealed mechanical stirrer, a gas-inlet tube, and a dry ice condenser protected from the air by a soda-lime drying tube (Note 1). The system is flushed thoroughly with dry ammonia, and 32.8 g. (0.84 mole) of sodium amide (Note 2) is added to the flask. The system is again flushed with ammonia, the condenser is provided with dry ice covered by acetone, and 1.2 l. of liquid…
Provide the conditions and show the curved arrow mechanism and Intermediate for the reactions leading to 1 or 2 selectively
Write suitable detailed mechanisms to account for the formation of the products in the following reactions, paying particular attention to clear drawings of structures and arrows as well as proper stoichiometry [WHERE APPROPRIATE]. You are required to show ALL intermediates and any by products that are formed in these reactions.
Suggest a synthesis for the molecule below starting from benzene, alcohols of four carbons or fewer and any inorganic reagents for questions D-H please provide the full names for the compounds below
Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(CzHs)3). 3SnCl4 + 4Al(C2H5)3 → 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d= 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
I need specific description of the compounds involved in the synthesis (functional groups, specific features). and also describe the steps involved in the synthesis and the role of each step. And most important！！devote one to each step of the synthesis. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesis
give the organic product/s of the following reactions (include stereochemistry where appropriate) , please help with all parts
can i get help drawing out actual structures including the nucleophilic addition of Cy2NH to parafomaldehyde and its hemiaminal intermidiate and the condensation step when it is displaced by terminal alkyne forming allene, also what is dioxane getting rid of as the solvent, thanks
An unknown hydrocarbon G, whose formula is C16H26 contains two triple bonds. Ozonolysis followed by reduction with (CH3)2S gave CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. Suggest a reasonable structure for compound G.
Give the synthesis mechanism for following molecule from methane, ethane or benzene. give clear handwritten solution!
Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides.One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(C2H5)3). 3SnCl4 + 4Al(C2H5)3 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.230 L of SnCl4 (d = 2.226 g/mL) was treated with 0.396 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). If 0.335 L of tetraethylstannane (d = 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?
Write suitable detailed mechanisms to account for the formation of the products in the following reactions, with arrows and proper stochiometry. Show all intermediates and any by products that are formed in these reactions.

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