please provide drawing with arrows Carbonyl Reactions Identify the Nucleophile and the Electrophile and THEN predict...
1. a) (6 points) For each of the following reactions, identify the nucleophile and the electrophile and draw the electron motion arrows required to generate the product given. nuc HOCH, HCH elec Hoe 09 OH CH OCH CH : ZEO: OCH,CH, ope
(a.) For each of the following reactions, identify the nucleophile and electrophile and draw the electron motion arrows required to generate the product given. (b.) The spectrum above was measured on a sample with molecular formula C4H7ClO2. In the box in the middle of the spectrum, draw the structure of a conpound with this formula that is consistent with the spectrum above (there are wuite a few structures that woukd fit). Do not attempt to match the fingerprint region. (c.)...
Supply the arrows for each of the following reactions. Identify the nucleophile/base and the electrophile/acid (when possible). Calcualte AH for each reaction. Estimate Keq (>1 or <1) for each reaction. Is the reaction exothermic or endothermic? You must answer all of the questions to receive full credit. Use the bond strength chart provided for bond dissociation energies. Upload answers (with your name clearly shown) as WORD, PDF or JPEG] Reaction 1 | 16-H 1 + + :NH, NH3 Reaction 2...
Predict the product of the reaction mechanisms. Identify the electrophile and nucleophile in each reaction. Propose a mechanism for each reaction below. This means show curved arrows. You may want to fill in any nonbonding electrons. Show an example of each of the following types of reactions and explain why it is that type: Addition elimination Rearrangement Substitution
Draw the mechanism for the previous 2 reactions. Remember arrows should go from nucleophile to electrophile. (Full: both mechanisms correct with no more than 1 minor error, partial: one mechanism correct with no more than 1 minor error OR both correct with no more than 3 minor errors) HNMR assignment, partial: correct NMR assignments) 460 OH 0.98 Br 0.98 \.92 (3.90 11.92 0.98 0.98 C7H 40 Reagents for Synthesis mg, Etzo 2 PPM 4.2 ppm, 1H, s 3.2 ppm, 1H,...
Please explain and show arrows if possible! Thank you! Q1) Identify the nucleophile and electrophile i ction below and label them. (10 poin + H-C + CT 3 points 'О CN 2. 3 points 3. 4 points
Predict whether they are nucleophiles, electrophile, oxidizing, reducing agent or none. 1) Predict whether each of the reagents would be primarily one of the following: a nucleophile, an electrophile, an oxidizing reagent, a reducing agent or none. (0.5 points each.) OsO4 H, KMnO4 CH3MgBr CH,-Cl C3Hg KOH NaCN For the following reactions, predict the major product. Assume that reagents dded are in excess when required. You do not need to show mechanisms (2 points ach). MgBr 1) 1) Predict whether...
Please show all arrows and explain the answer Predict the Product. Provide the stable organic product(s) for the reactions below. MgBr (1 eq.) von 1. Mgº, CH3CH2OCH2CH3 2. Å 3. H2O, HCI 1. CH,MgBr (xs) 2. H2O, HCI 1. Mg", CH3CH,OCH,CH3 2. D20
(d) Complete the following reactions by drawing the structure in the boxes provided of the carbonyl compound required for each reaction. Complete the following reactions by drawing the structure in the b provided of the carbonyl compound required for each reaction oxes (d) HO MgBr 1. 2. НО он MgBr 1. Excess 2. НО
Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. 53) Reaction of the following with HBr in electrophilic addition reactions Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction) yo...