Chemistry Atoms First2e
2nd Edition
ISBN: 9781947172647
Author: OpenStax
Publisher: OpenStax College
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Textbook Question
Chapter 19, Problem 4E
Why are the lanthanoid elements not found in nature in their elemental forms?
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Highlight each glycosidic bond in the molecule below. Then answer the questions in the table under the drawing area.
HO-
HO-
-0
OH
OH
HO
NG
HO-
HO-
OH
OH
OH
OH
NG
OH
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Suppose the molecule in the drawing area below were reacted with H₂ over a platinum catalyst. Edit the molecule to show what would happen to it. That is, turn
it into the product of the reaction.
Also, write the name of the product molecule under the drawing area.
Name: ☐
H
C=0
X
H-
OH
HO-
H
HO-
-H
CH₂OH
×
Draw the Haworth projection of the disaccharide made by joining D-glucose and D-mannose with a ẞ(1-4) glycosidic bond. If the disaccharide has more than
one anomer, you can draw any of them.
Click and drag to start drawing a
structure.
X
Chapter 19 Solutions
Chemistry Atoms First2e
Ch. 19 - Write the electron configurations far each of the...Ch. 19 - Write the electron con?gurations for each of the...Ch. 19 - Write the electron configurations for each of the...Ch. 19 - Why are the lanthanoid elements not found in...Ch. 19 - Which of the following elements is most likely to...Ch. 19 - Which of the following is the strongest oxidizing...Ch. 19 - Which of the following elements is most likely to...Ch. 19 - The following reactions all occur in a blast...Ch. 19 - Why is the formation of slag useful during the...Ch. 19 - Would you expect an aqueous manganese (VII) oxide...
Ch. 19 - Iron (II) can be oxidized to iron (III) by...Ch. 19 - How many cubic feet of air at a pressure of 760...Ch. 19 - Find the potentials of the following...Ch. 19 - A 2.5624-g sample of a pure solid alkali metal...Ch. 19 - The standard reduction potential for the reaction...Ch. 19 - Predict the products of each of the following...Ch. 19 - Predict the products of each of the following...Ch. 19 - Describe the electrolytic process for refining...Ch. 19 - Predict the products of the following reactions...Ch. 19 - What is the gas produced when iron(II) sulfide is...Ch. 19 - Predict the products of each of the following...Ch. 19 - Balance the following equations by...Ch. 19 - Dilute sodium cyanide solution is slowly dripped...Ch. 19 - Predict which will be more stable, [CrO4]2- or...Ch. 19 - Give the oxidation state of the metal for each of...Ch. 19 - Indicate the coordination number for the central...Ch. 19 - Give the coordination numbers and write the...Ch. 19 - Give the coordination number for each metal ion in...Ch. 19 - Sketch the structures of the following complexes....Ch. 19 - Draw diagrams for any Cis, trans, and optical...Ch. 19 - Name each of the compounds or ions given in...Ch. 19 - Name each of the compounds or ions given in...Ch. 19 - Specify whether the following complexes have...Ch. 19 - Predict whether the carbonate ligand CO32- will...Ch. 19 - Draw the geometric, linkage, and ionization...Ch. 19 - Determine the number of unpaired electrons...Ch. 19 - Draw the Crystal field diagrams for [Fe(NO2)6]4-...Ch. 19 - Give the oxidation state of the metal, number of d...Ch. 19 - The solid anhydrous solid CoCl2 is blue in color....Ch. 19 - Is it possible for a complex of a metal in the...Ch. 19 - How many unpaired electrons are present in each of...Ch. 19 - Explain how the diphosphate ion, [O3P-O-PO3]4-,...Ch. 19 - For complexes of the same metal ion with no change...Ch. 19 - Trimethylphosphine, P(CH3)3, can act as a ligand...Ch. 19 - Would you expect the complex [Co(en)3]Cl3 to have...Ch. 19 - Would you expect the Mg3[Cr(CN)5]2 to be...Ch. 19 - Would you expect salts of the gold(I) ion, Au+, to...Ch. 19 - [CuCl4]2- is green. [Cu(H2O)6]2+ is blue. Which...
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- Epoxides can be opened in aqueous acid or aqueous base to produce diols (molecules with two OH groups). In this question, you'll explore the mechanism of epoxide opening in aqueous acid. 2nd attempt Be sure to show all four bonds at stereocenters using hash and wedge lines. 0 0 Draw curved arrows to show how the epoxide reacts with hydronium ion. 100 +1: 1st attempt Feedback Be sure to show all four bonds at stereocenters using hash and wedge lines. See Periodic Table See Hint H A 5 F F Hr See Periodic Table See Hintarrow_forward03 Question (1 point) For the reaction below, draw both of the major organic products. Be sure to consider stereochemistry. > 1. CH₂CH₂MgBr 2. H₂O 3rd attempt Draw all four bonds at chiral centers. Draw all stereoisomers formed. Draw the structures here. e 130 AN H See Periodic Table See Hint P C Brarrow_forwardYou may wish to address the following issues in your response if they are pertinent to the reaction(s) you propose to employ:1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Please make it in detail and draw it out too in what step what happens. Thank you for helping me!arrow_forward
- 1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Everything in detail and draw out and write it.arrow_forwardCalculating the pH at equivalence of a titration 3/5 Izabella A chemist titrates 120.0 mL of a 0.7191M dimethylamine ((CH3)2NH) solution with 0.5501 M HBr solution at 25 °C. Calculate the pH at equivalence. The pk of dimethylamine is 3.27. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of HBr solution added. pH = ☐ ✓ 18 Ar Boarrow_forwardAlcohols can be synthesized using an acid-catalyzed hydration of an alkene. An alkene is combined with aqueous acid (e.. sulfuric acid in water). The reaction mechanism typically involves a carbocation intermediate. > 3rd attempt 3343 10 8 Draw arrows to show the reaction between the alkene and hydronium ion. that 2nd attempt Feedback 1st attempt تعمال Ju See Periodic Table See Hint F D Ju See Periodic Table See Hintarrow_forward
- Draw the simplified curved arrow mechanism for the reaction of acetone and CHgLi to give the major product. 4th attempt Π Draw the simplified curved arrow mechanism T 3rd attempt Feedback Ju See Periodic Table See Hint H -H H -I H F See Periodic Table See Hintarrow_forwardSelect the correct reagent to accomplish the first step of this reaction. Then draw a mechanism on the Grignard reagent using curved arrow notation to show how it is converted to the final product. 4th attempt Part 1 (0.5 point) Select the correct reagent to accomplish the first step of this reaction. Choose one: OA Mg in ethanol (EtOH) OB. 2 Li in THF O C. Li in THF D. Mg in THF O E Mg in H2O Part 2 (0.5 point) Br Part 1 Bri Mg CH B CH, 1 Draw intermediate here, but no arrows. © TE See Periodic Table See Hint See Hint ין Harrow_forwardSelect the product for the following reaction. HO HO PCC OH ○ OH O HO ○ HO HO HOarrow_forward
- 5:45 Х Select the final product for the following reaction sequence. O O 1. Mg. ether 2.D.Oarrow_forwardBased on the chart Two similarities between the molecule with alpha glycosidic linkages. Two similarities between the molecules with beta glycosidtic linkages. Two differences between the alpha and beta glycosidic linkages.arrow_forwardplease help fill in the tablearrow_forward
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