CHEMICAL PRINCIPLES PKG W/SAPLING
7th Edition
ISBN: 9781319086411
Author: ATKINS
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Videos
Question
Chapter 1, Problem 1D.2AST
Interpretation Introduction
Interpretation:
The type of orbital that corresponds to the following sets of quantum numbers has to be predicted.
Concept introduction:
Quantum numbers: These terms explains the distribution of electron density in an atom. They are derived from Schrodinger's equation’s solution for the hydrogen atom. The four types of quantum numbers are the principal quantum number
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Write the systematic name of each organic molecule:
structure
요
OH
ہو۔
HO
OH
name
X
S
☐
☐
Predict the major products of this organic reaction.
If there aren't any products, because nothing will happen, check the box under the drawing area instead.
D
ㄖˋ
ید
H
No reaction.
+
5
H₂O.*
Click and drag to start
drawing a structure.
OH
H₂O
Draw one product of an elimination reaction between the molecules below.
Note: There may be several correct answers. You only need to draw one of them. You do not need to draw any of the side products of the reaction
'O
10
+
x
也
HO
+
义
Click and drag to start
drawing a structure.
Chapter 1 Solutions
CHEMICAL PRINCIPLES PKG W/SAPLING
Ch. 1 - Prob. 1A.1ASTCh. 1 - Prob. 1A.1BSTCh. 1 - Prob. 1A.2ASTCh. 1 - Prob. 1A.2BSTCh. 1 - Prob. 1A.1ECh. 1 - Prob. 1A.3ECh. 1 - Prob. 1A.4ECh. 1 - Prob. 1A.5ECh. 1 - Prob. 1A.6ECh. 1 - Prob. 1A.7E
Ch. 1 - Prob. 1A.8ECh. 1 - Prob. 1A.9ECh. 1 - Prob. 1A.10ECh. 1 - Prob. 1A.11ECh. 1 - Prob. 1A.12ECh. 1 - Prob. 1A.13ECh. 1 - Prob. 1A.14ECh. 1 - Prob. 1A.15ECh. 1 - Prob. 1A.16ECh. 1 - Prob. 1A.17ECh. 1 - Prob. 1B.1ASTCh. 1 - Prob. 1B.1BSTCh. 1 - Prob. 1B.2ASTCh. 1 - Prob. 1B.2BSTCh. 1 - Prob. 1B.3ASTCh. 1 - Prob. 1B.3BSTCh. 1 - Prob. 1B.4ASTCh. 1 - Prob. 1B.4BSTCh. 1 - Prob. 1B.5ASTCh. 1 - Prob. 1B.5BSTCh. 1 - Prob. 1B.1ECh. 1 - Prob. 1B.2ECh. 1 - Prob. 1B.3ECh. 1 - Prob. 1B.4ECh. 1 - Prob. 1B.5ECh. 1 - Prob. 1B.6ECh. 1 - Prob. 1B.7ECh. 1 - Prob. 1B.8ECh. 1 - Prob. 1B.9ECh. 1 - Prob. 1B.10ECh. 1 - Prob. 1B.11ECh. 1 - Prob. 1B.12ECh. 1 - Prob. 1B.13ECh. 1 - Prob. 1B.14ECh. 1 - Prob. 1B.15ECh. 1 - Prob. 1B.16ECh. 1 - Prob. 1B.17ECh. 1 - Prob. 1B.18ECh. 1 - Prob. 1B.19ECh. 1 - Prob. 1B.21ECh. 1 - Prob. 1B.22ECh. 1 - Prob. 1B.23ECh. 1 - Prob. 1B.24ECh. 1 - Prob. 1B.25ECh. 1 - Prob. 1B.26ECh. 1 - Prob. 1B.27ECh. 1 - Prob. 1B.28ECh. 1 - Prob. 1C.1ASTCh. 1 - Prob. 1C.1BSTCh. 1 - Prob. 1C.1ECh. 1 - Prob. 1C.2ECh. 1 - Prob. 1C.3ECh. 1 - Prob. 1C.7ECh. 1 - Prob. 1D.1ASTCh. 1 - Prob. 1D.1BSTCh. 1 - Prob. 1D.2ASTCh. 1 - Prob. 1D.2BSTCh. 1 - Prob. 1D.1ECh. 1 - Prob. 1D.2ECh. 1 - Prob. 1D.3ECh. 1 - Prob. 1D.4ECh. 1 - Prob. 1D.5ECh. 1 - Prob. 1D.6ECh. 1 - Prob. 1D.7ECh. 1 - Prob. 1D.9ECh. 1 - Prob. 1D.10ECh. 1 - Prob. 1D.11ECh. 1 - Prob. 1D.12ECh. 1 - Prob. 1D.13ECh. 1 - Prob. 1D.14ECh. 1 - Prob. 1D.15ECh. 1 - Prob. 1D.16ECh. 1 - Prob. 1D.17ECh. 1 - Prob. 1D.18ECh. 1 - Prob. 1D.19ECh. 1 - Prob. 1D.20ECh. 1 - Prob. 1D.21ECh. 1 - Prob. 1D.22ECh. 1 - Prob. 1D.23ECh. 1 - Prob. 1D.24ECh. 1 - Prob. 1D.25ECh. 1 - Prob. 1D.26ECh. 1 - Prob. 1E.1ASTCh. 1 - Prob. 1E.1BSTCh. 1 - Prob. 1E.2ASTCh. 1 - Prob. 1E.2BSTCh. 1 - Prob. 1E.1ECh. 1 - Prob. 1E.2ECh. 1 - Prob. 1E.3ECh. 1 - Prob. 1E.4ECh. 1 - Prob. 1E.5ECh. 1 - Prob. 1E.7ECh. 1 - Prob. 1E.8ECh. 1 - Prob. 1E.9ECh. 1 - Prob. 1E.10ECh. 1 - Prob. 1E.11ECh. 1 - Prob. 1E.12ECh. 1 - Prob. 1E.13ECh. 1 - Prob. 1E.14ECh. 1 - Prob. 1E.15ECh. 1 - Prob. 1E.16ECh. 1 - Prob. 1E.17ECh. 1 - Prob. 1E.18ECh. 1 - Prob. 1E.19ECh. 1 - Prob. 1E.20ECh. 1 - Prob. 1E.21ECh. 1 - Prob. 1E.22ECh. 1 - Prob. 1E.23ECh. 1 - Prob. 1E.24ECh. 1 - Prob. 1E.25ECh. 1 - Prob. 1E.26ECh. 1 - Prob. 1F.1ASTCh. 1 - Prob. 1F.1BSTCh. 1 - Prob. 1F.2ASTCh. 1 - Prob. 1F.2BSTCh. 1 - Prob. 1F.3BSTCh. 1 - Prob. 1F.1ECh. 1 - Prob. 1F.2ECh. 1 - Prob. 1F.3ECh. 1 - Prob. 1F.4ECh. 1 - Prob. 1F.5ECh. 1 - Prob. 1F.6ECh. 1 - Prob. 1F.7ECh. 1 - Prob. 1F.8ECh. 1 - Prob. 1F.10ECh. 1 - Prob. 1F.11ECh. 1 - Prob. 1F.12ECh. 1 - Prob. 1F.13ECh. 1 - Prob. 1F.14ECh. 1 - Prob. 1F.15ECh. 1 - Prob. 1F.17ECh. 1 - Prob. 1F.18ECh. 1 - Prob. 1F.19ECh. 1 - Prob. 1F.22ECh. 1 - Prob. 1.1ECh. 1 - Prob. 1.2ECh. 1 - Prob. 1.3ECh. 1 - Prob. 1.9ECh. 1 - Prob. 1.10ECh. 1 - Prob. 1.11ECh. 1 - Prob. 1.12ECh. 1 - Prob. 1.13ECh. 1 - Prob. 1.14ECh. 1 - Prob. 1.15ECh. 1 - Prob. 1.17ECh. 1 - Prob. 1.19ECh. 1 - Prob. 1.21ECh. 1 - Prob. 1.22ECh. 1 - Prob. 1.23ECh. 1 - Prob. 1.24ECh. 1 - Prob. 1.25ECh. 1 - Prob. 1.27ECh. 1 - Prob. 1.28ECh. 1 - Prob. 1.31E
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- What are the angles a and b in the actual molecule of which this is a Lewis structure? H- :0: C=N: b Note for advanced students: give the ideal angles, and don't worry about small differences from the ideal that might be caused by the fact that different electron groups may have slightly different sizes. a = 0° b=0 Xarrow_forwardA student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. • If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. + This transformation can't be done in one step. T iarrow_forwardDetermine the structures of the missing organic molecules in the following reaction: H+ O OH H+ + H₂O ☑ ☑ Note: Molecules that share the same letter have the exact same structure. In the drawing area below, draw the skeletal ("line") structure of the missing organic molecule X. Molecule X shows up in multiple steps, but you only have to draw its structure once. Click and drag to start drawing a structure. X § ©arrow_forward
- Table 1.1 Stock Standard Solutions Preparation. The amounts shown should be dissolved in 100 mL. Millipore water. Calculate the corresponding anion concentrations based on the actual weights of the reagents. Anion Amount of reagent (g) Anion Concentration (mg/L) 0.1649 Reagent Chloride NaCl Fluoride NaF 0.2210 Bromide NaBr 0.1288 Nitrate NaNO3 0.1371 Nitrite NaNO2 0.1500 Phosphate KH2PO4 0.1433 Sulfate K2SO4 0.1814arrow_forwardDraw the structure of the pound in the provided CO as a 300-1200 37(2), 11 ( 110, and 2.5 (20arrow_forwardPlease help me with # 4 and 5. Thanks in advance!arrow_forward
- A small artisanal cheesemaker is testing the acidity of their milk before it coagulates. During fermentation, bacteria produce lactic acid (K₁ = 1.4 x 104), a weak acid that helps to curdle the milk and develop flavor. The cheesemaker has measured that the developing mixture contains lactic acid at an initial concentration of 0.025 M. Your task is to calculate the pH of this mixture and determine whether it meets the required acidity for proper cheese development. To achieve the best flavor, texture and reduce/control microbial growth, the pH range needs to be between pH 4.6 and 5.0. Assumptions: Lactic acid is a monoprotic acid H H :0:0: H-C-C H :0: O-H Figure 1: Lewis Structure for Lactic Acid For simplicity, you can use the generic formula HA to represent the acid You can assume lactic acid dissociation is in water as milk is mostly water. Temperature is 25°C 1. Write the K, expression for the dissociation of lactic acid in the space provided. Do not forget to include state symbols.…arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :0: :0 H. 0:0 :0: :6: S: :0: Select to Edit Arrows ::0 Select to Edit Arrows H :0: H :CI: Rotation Select to Edit Arrows H. < :0: :0: :0: S:arrow_forward3:48 PM Fri Apr 4 K Problem 4 of 10 Submit Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Mg. :0: Select to Add Arrows :0: :Br: Mg :0: :0: Select to Add Arrows Mg. Br: :0: 0:0- Br -190 H 0:0 Select to Add Arrows Select to Add Arrows neutralizing workup H CH3arrow_forward
- Iarrow_forwardDraw the Markovnikov product of the hydrobromination of this alkene. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for this problem. + Explanation Check 1 X E 4 1 1 1 1 1 HBr Click and drag to start drawing a structure. 80 LE #3 @ 2 $4 0 I அ2 % 85 F * K M ? BH 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center & 6 27 FG F10 8 9 R T Y U D F G H P J K L Z X C V B N M Q W A S H option command H command optiarrow_forwardBe sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. Predict the major products of the following reaction. Explanation Q F1 A Check F2 @ 2 # 3 + X 80 F3 W E S D $ 4 I O H. H₂ 2 R Pt % 05 LL ee F6 F5 T <6 G Click and drag to start drawing a structure. 27 & A 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center Acce Y U H DII 8 9 F10 4 J K L Z X C V B N M T H option command F11 P H commandarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Quantum Numbers, Atomic Orbitals, and Electron Configurations; Author: Professor Dave Explains;https://www.youtube.com/watch?v=Aoi4j8es4gQ;License: Standard YouTube License, CC-BY
QUANTUM MECHANICAL MODEL/Atomic Structure-21E; Author: H to O Chemistry;https://www.youtube.com/watch?v=mYHNUy5hPQE;License: Standard YouTube License, CC-BY