number 3 please thank you Activity 3: Chem 333D, 11/4 or 6/19 (Please do not explain...
any help is appreciated thank you Activity 3: Chem 333D, 11/4 or 6/19 (Please do not explain any of the answers in more than 3 sentences) Name: 1.) What makes an atom a good nucleophile? (3 points) 2.) What makes an atom a good electrophile? (3 points) 3.) What factors influence if a reaction is going to be a substitution or elimination reaction? (4 points)
Activity 4: Chem 334 MW, 1114/19 (it is recommended you show as much work as possible for partial credit) Name: 11.) Provide the mechanism for each step and the final product for the following series of reactions. (5 points) 1.) excess CH31 2.) Ag,0,H,O, A 13.) Provide the mechanism for each step and the final product for the following series of reactions. (25 points) 1.) HNO/H2SO4 2.) Zn (Hg), HCI 3.) HNO/HCI 4.) H30, A 5.) O o
Please explain, thank you! WW2 Online teaching MindTap.Cengage Learn Activity Stream X G proton transfer organic ch x + - 0 comintakeAssignment take covalentActivity.do?locator assignment-take&take AssignmentSessionLocator assignment-take TReview Topics] (References] _1 pts + H2O 1 pts OCH + ze 1 pts Brz + Her a = Proton transfer b = Lewis acid base c = Radical chain substitution d = Radical chain addition e-Electrophile addition f=E1 Elimination g=E2 Elimination h=Sx 1 Nucleophilic substitution i=SN2 Nucleophilic substitution j = Electrophilie aromatic...
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
Please show steps to reactions/show work, thank you! Chem 322 Problem Set 4 Due to Dr. Hietbrink by 3:00 on Monday 4-8-19 Circle your class: MWF 11:15, MWF 12:20, TTh 2:00 Fill in the missing compounds (1 point each) Name Class student # Score (out of 10) H2CrO4: a) LDA a) LDA : a) KOH 2) a) CH3MgBr PCC 3) b) Ht AICI a)LDA c) H, hot ...' a) DCC
Name Chem 321 - Problem Set 6 Due to Dr. Hietbrink by 3:00 on Mon 11-18-19 Circle your class: MWF 11:15, MWF 12:20, TTh 2:00 Student number Score (out of 10) 1. (10 points) Predict the major organic product or products for each of the following. Be sure to include stereochemistry where appropriate. Assume each is in the most appropriate solvent. Remember, "no reaction" may be an answer. a) O, b) DMS HgSO4 H2SO4 НО B2 HCI a)/MOBI b) H
Can someone help me with both of these, id appreciate it THANK YOU!!!!!! 3. For the following reaction, please draw the transition state of the rate-limiting step CH2CH3 CH3OH "H H2SO4, 25 °C in the rate- 4. What are the electrophile and the nucleophile limiting step of the following reaction? Lo hamon HCI
Organic Chem Ch 11 worksheet Name Homework #7 20 Points Due 11/20/19 1) Name the following (6 points) NH2 он 2) Draw the following (4 points) (1R)-1-bromo-N-methylpentan-1-amine (2R)-2-cyanopropanoic acid 3) What are the products and mechanisms for both products? (4 points) HBr Thermodynamic Kinetic 4) Fill-in the Boxes (6 points) НCL Br Only Products Br 1) LDA (2X) 2) H2SO4, HgSO, H20 НВr, -80°C One Product
CHEM 330 Homework # 9 Name: Due: 11/06/19 Identify which of the following two reactions you would expect to occur more rapidly and then explain your choice. (2 pts) 4. НЕг HЕг 5. Suggest an efficient target synthesis for the following transformation. (3 pts) OH 2 steps Br Provide the complete mechanism for the following reaction. (6 pts) 6 но HаРОд Н-о
Please explain. Thank you. (4) (16 points) Write the name of the shape of these ions; the central atom is written first. (a) SF5 (b) XeFO2- (c) CIF 4+ (d) IF2+