If you used a large excess of Br2 and FeBr3, what structure would result from the bromination of N-ethyl phenothiazine?
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If you used a large excess of Br2 and FeBr3, what structure would result from the...
3. Draw the stereoisomeric structure of the products that you would expect from the bromination of the following Compounds using Br2 in CCl4. Use sawhorse projections. A. cis-3-hexene B. trans-3-hexene
&H5 H What Rand/or S configuration would be used for the following structure? 10 pts Br H и соодносно HC Tonic OH .AH CH N HOĆ (CH3)CH CH=CH2
Thank you! 9. What would be the product of the following conversion? 1. NaOEt, EIOH OEt 2. H,о- OEt ОН О OEt OEt OEt OE OEt e. d. 10. What is the product of the Dieckmann condensation of the following diester? 1.NaOCH, CH,Oн HgCOoc coOCHs 2. H,0* осн, COOCH COOCH b. d. both a) and b) e. a), b), and c) a. C. 11. Consider the synthesis below. What is compound X? COOEt COOH 1. КОВи 1. NAOH, H2O, heat...
This is for Organic II. Thank you! Give the primary product that would result from the following reactions: NOTE: If the problem involves multiple reactions, and you cannot determine the final product, draw the structure of any of the intermediate products (and indicate which reaction the product is for, i.e. Step # 1 , Step # 2 , etc.) 1) BHs, THF 2) н.о,. он-) 3) (CH3)2NH 4) H2, Pt/C Cat. н. он N-CH3 b) 1) н,о'*) 2) Na2Cr o,,...
2) Provide the structure of the product that will result from the treatment of malonic ester (also known as diethyl malonate) successively with sodium ethoxide, ethyl bromide, potassium t-butoxide, isobutyl chloride, followed by aqueous HCl and heat
1) What are the products of the following sequence of reactions? Write the structure of the intermediates (reaction with Mg), and the structure of the final product. 1) Mg, Diethyl ether Н,о A Br A) 2-butanol and MgHBr C) butane and Mg(OH)Br B) butane and MgHBr D) 2-butanol and Mg(OH)Br 2) What is the major product of the following reaction? Write the structures of intermediates and the products. 2) Mg, Diethyl ether 1. Н.С-о 2. H20* Br B) 2-ethyl-1-pentanol D)...
4. What theoretical mass of NaCl would result from reacting 6.20 g of Na2CO, with excess HCl(aqueous)? Show your work.
please help with filling out this table and answering 8 questions Data Table Br H CH2CH3OH N-H Bry Chemicals H (E)-Stilbene Ethanol Pyridinium tribromide CsH.Br3N Stilbene Dibromide C14H12Br2 Molecular Formula C14H12 CHO Molecular Weight 180.25 g/mol 46.07 g/mol 319.82 g/mol 340.06 g/mol Physical Properties White solid Clear liquid White solid White solid Melting Point 122-124 °C N/A 127-133 °C 241-243 °C Amount needed 0.25 g 10 mL 0.5 g Mole needed 1.39 mmol 1.56 mmol Amount Used Moles Used Amount...
2. Your lab manual proposes 3 possible mechanisms for bromination. During this lab, you will determine which iroduct(s) formed during the bromination of stilbene. (9 pts) a. Four possible products from the bromination of trans-stilbene are shown below. Label the chiral centers as Sor R. Ph Br Br H iph H Phil Br Ph Ph Br B. HINH Philiph Phí By HP b. The enantiomer of structure A is: c. The enantiomer of structure Dis: d. Ust the letters corresponding...
1. Draw the chemical structure of veratrole. What is the mass of veratrole being used in this reaction? осн 2. How many unique mononitrated products of veratrole can theoretically be produced (regardless of the directing abilities of the substituents present)? Draw these potential products. 3. What kind of director (ortho/para, meto, etc.) are the substituents on veratrole? 4. Predict the major product(s) of the following reactions using the principles taught in class. Assume all reagents are present in 1:1 ratios...