Provide the product(s) and mechanism for the following reactions. Include all intermediates, resonance structures, charges, and electron pushing arrows to obtain full credit.
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Solution:
The products and missing reagents for the reactions are given below with their mechanism.
Provide the product(s) and mechanism for the following reactions. Include all intermediates, resonance structures, charges, and...
4. Provide a stepwise mechanism. Include all intermediates, resonance structures, and electron pushing arrows.(ALL OR NOTHING) HEC CH3 AICI D. HCI 5. (Provide the product(s) or reagent(s) for the following reactions. COM ????? ON 77277 HON C ?????
Provide a full mechanism for the following reaction. Include intermediates, formal charges, and curved arrows to show electron flow. Provide a full mechanism for the following reaction. Include intermediates, formal charges, and curved arrows to show electron flow. H20, H о нон, он вме OH HN
Provide a full mechanism for the synthesis of 3-acetyl-7-(diethylamino)-2H-1-benzopyran-2-one. Include all formal charges, resonance structures, intermediates and products. Use proper arrows for electron flow, vaguely drawn arrows will not receive marks.
Predict the product or provide the mechanism Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH,OCH CH3 2. CO2 (g) 3. H2O, HCI W MgBr (xs) 2. H2O, HCI 1. K Cr2O7, H2SO4, H2O 2. CH3MgBr (1 eq.) OH 3. H2O, HCI 1. Mgº, CH3CH2OCH2CH3 2. H2O, HCI Mechanism. The following Grignard reaction has been observed to yield products A and B. 1. Me Me MCI THF, -70 °C SOH OH ole er periodo...
3. (25 points) All six membered ring sugars, in the presence of acid and a nucleophile, proceed via an Sn1 mechanism to yield only 1 product (as shown below). A) Provide a mechanism for the following reaction. Include all intermediates, resonance structures, charges, and electron pushing arrows to obtain full credit. B Why does the reaction not occur at the other 4 possible positions where there are alcohols? You may use mechanisms or intermediates to explain your answer. ООН OCH,...
1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 он +H20 HCI
1. Determine which of the following compounds are aromatic or antiaromatic. SHOW CALCULATIONS! 2. Provide the product and a stepwise mechanism for the following reaction. Include all intermediates, resonance structures, and electron pushing arrows. 1. (4 points) Determine which of the following compounds are aromatic or anti- aromatic. SHOW CALCULATIONS! 0: O NO 0: 2. (8 points) Provide the product and a stepwise mechanism for the following reaction. Include all intermediates, resonance structures, and electron pushing arrows. OHC CH3NH2 CI
Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. 1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
Predict the product CONCEPT QUESTION Predict the Product. Provide the stable organic product(s) for the reactions below MgBr (1 eq.) но 1. Mgo, CH3CH20CH2CH3 2. 3. НаО, HСІ Mechanism. Provide the complete mechanism for the following transformation. You must include appropriate arrows, intermediates, and formal charges. MgCl 1 но 2. H2О, HСI
For the mechanism, show all the steps with multiple reaction arrows, electron arrows, formal charges, etc. CONCEPT QUESTIONS Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH2OCH,CH3 2. CO2 (g) 3. H20, HCI 1. MgBr (1eq.) 2. H20, HCI Mechanism. Using ChemDraw, provide the complete mechanism for the following transformation. You must include appropriate arrows, intermediates, and formal charges. 1. MgCI 2. H20, HCI