6. (4 pts. total; 2 pts, each) For each of the following questions, circle the BEST answer. a. Strongest Bronsted-L...
show all work please thank you!! 6. (4 pts total; 2 pts, each) For each of the following questions, circle the BEST answer a. Strongest Bronsted-Lowry acid HF HCI HBr b. Has the lowest pka CHA NH Hao HAS 7. (4 pts total, 2 pts each) For each of the following molecular structures, circle the MOST acidic hydrogen. Note that lone pairs have been omitted for clarity. HH нннн HANC COH HHH HH
6 (4 pts, total: 2 pts, each) For each of the following questions, circle the BEST a. Strongest Bronsted-Lowry acid HF HCI HBO HI b. Has the lowest pk. CH NH H2O Has 7. (4 pts total, 2 pts each) For each of the following molecular structures, circle the MOST acidic hydrogen. Note that lone pairs have been omitted for clarity. HH HHHH Horacaugh a HHH b Hн 8. (4 pts. total; 2 pts, each) in the space provided below,...
6. (4 pts. total 2 pts.cach) For each of the following questions, circle the BEST answer a Strongest Bronsted-Lowry acid нсі HB: HF b. Has the lowest pk. CHA NH3 H20 Has 7. (4 pts total, 2 pts each) For each of the following molecular structures, circle the MOST acidie hydrogen. Note that lone pairs have been omitted for clarity. HH н ннн нссон Hagh HHH HH 8. (4 pts. total: 2 pts, each) In the space provided below, explain...
(6 pts total: 2 pts each) Proteins that catalyze chemical reactions in living systems are called enzymes. The basic building blocks of proteins are called amino acids and have the general structure pictured below, left, where R is a substituent containing one of many organic functional groups. Some representative examples of amino acids found in nature are pictured here as well (R groups only) O . CH, HO-C-H H-C-H HẠC-C-CH, CH,SH HNT-CO,H Cysteine Valine Threonine Aspartic Acid An Amino Acid...
1. (6 pts total; 2 pts each) Proteins that catalyze chemical reactions in living systems are called enzymes. The basic building blocks of proteins are called amino acids and have the general structure pictured below, left, where R is a substituent containing one of many organic functional groups. Some representative examples of amino acids found in nature are pictured here as well (R groups only) сн. н 0:00 HO-C-H. HỌC-C-CH, CH,SH H-C-H H2N -CO,H H An Amino Acid Threonine Valine...
4. Consider phosphonic acid, an inorganic acid that has both the empirical and molecular formua HaPOs... a. (4 pts) Draw the most stable Lewis electron dot structure for HaPOs containing one double bond and no formal charges. Place your answer in the space provided. HaPOs with one double bond b. (3 pts) What is the orbital hybridization at phosphorus in your answer to part (a)? (4 pts) Draw the most stable Lewis electron dot structure for HaPOs containing no double...
(4 pts) 6. For each of the following conjugate-acid, and the conjugate-base pairs. Bronsted-Lowry acid caving reactions, dentity the Bronsted-Lowry acid,Bronsted-Lowry base, and the NH(aq)F(aq) b) CN(ag)+H
answer questions 13. If K-2.0x 10" at 25 C, for the following reaction: H2 (g)+ Cl(g) 2 HCI (g), then find Kp at the same temperature. (2 pts) 14. (a) Give the formula of the conjugate base of the following Bronsted-Lowry acids: (4pts) (i) HO (ii) H2CO (b) Give the formula of the conjugate acid of the following Bronsted-Lowry bases: (4pts) HSO (ii) NH 15. Identify the stronger acid in each of the following pairs and briefly explain the reason...
ave the (4 pt) pKa 1.96 рКа 9,89 acid (HCHO2), pKa 3.74 5. Circle the strongest acid in each of the following groups (rows). (18 pt) a. H2S H20 H2Se НЕТе b. H20 HF CH4 NH3 C Hхо4 HXO2 нхоз HXO d. HAtO HCIO HIO HBro NH4 CsHsNH CoHsNH3 e. NHs, Ko 1.8x10- CSHSNH, K 1.7x10- CaHsNHa, K = 3.8 x 10-1 OH OH OH OH 6. Three oxoacids with the formular il strength:
8. (4 pts. total; 2 pts. each) in the space provided below, explain the following atomic properties. Be succinct. Electronegativity (X) Polarizability 9. (4 pts) Trifluoroacetic acid (CF3CO2H; pka = 0.23) and acetic acid (CH3CO2H;pka = 4.75) are monoprotic acids (meaning they can dissociate only one H ion/molecule of acid). Using your knowledge of structure, explain why the acid dissociation (K) of acetic acid is greater than that for trifluoroacetic acid. Place your answer in the space provided.