![ALEKS 360 for Silberberg Chemistry: The Molecular Nature of Matter and Change](https://www.bartleby.com/isbn_cover_images/9781260477313/9781260477313_largeCoverImage.gif)
(a)
Interpretation:
The name of the given compound has to be given.
Concept Introduction:
The hydrocarbons which contain only single bonds are said to be
The Alkanes are named following some rules:
- The name of the alkane is given by the number of carbon atoms present in the chain. It is said to be Root of the alkane.
Root = number of carbon atoms in chain.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The root name is followed by Suffix. Suffix indicates the
functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(b)
Interpretation:
The name of the given compound has to be given.
Concept Introduction:
The hydrocarbons which contain only single bonds are said to be cycloalkanes. The general formula for alkanes can be given as
The cycloalkanes are named following some rules:
- The name of the alkane is given by the number of carbon atoms present in the ring. It is said to be Root of the alkane.
Root = number of carbon atoms in ring.
- To name the root, for one carbon atom, the root name use is meth-. For two carbon atoms, the root name is eth-, for three carbon atoms, it is prop-, for four carbon atoms, it is but-, for five carbon atoms, it is pent- and so on.
- The root name is followed by Suffix. Suffix indicates the functional group present in the compound. It is placed after the root name.
Suffix = name of the functional group present in the compound.
- The root name also contains Prefix. Prefix is the groups attached to the root. It indicates the branched carbon atoms on the root chain and name according to the root specifying the carbon number on which it is placed. It contains –yl in name end. The prefix is placed before the root name.
Prefix = name of the branched carbon atoms on chain.
- The name of the alkane is given in the form
Prefix + Root + Suffix
(c)
Interpretation:
The structure of the given compound (1,2-diethylcyclopentane) has to be drawn.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
(b)
Interpretation:
The structure of the given compound (2,4,5-trimethylnonane) has to be drawn.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 15 Solutions
ALEKS 360 for Silberberg Chemistry: The Molecular Nature of Matter and Change
- I need help working this problem out step by step, I was trying to use my example from the txt book but all I know how to do is set it up. I need to be shown step by step as I am a visual learner. Please help me.arrow_forwardDon't used hand raitingarrow_forwardDon't used Ai solution and don't used hand raitingarrow_forward
- & Calculate the molar enthalpy of combustion (A combH) of 1.80 g of pyruvic acid (CH3COCOOH; 88.1 g mol-1) at 37 °C when they are combusted in a calorimeter at constant volume with a calorimeter constant = 1.62 kJ °C-1 and the temperature rose by 1.55 °C. Given: R = 8.314 J mol −1 °C-1 and the combustion reaction: AN C3H4O3 + 2.502(g) → 3CO2(g) + 2H2O(l)arrow_forwardAn unknown salt, AB, has the following precipitation reaction:A+(aq) + B-(aq) ⇌ AB(s) the K value for this reaction is 4.50 x10-6. Draw a model that represents what will happen when 1.00 L each of 1.00 M solution of A+(aq) and 1.00M solution of B-(aq) are combined.arrow_forward5. a) Use the rules in Example 4.4 (p. 99) and calculate sizes of octahedral and tetrahedral cavities in titanium and in zirconium. Use values for atomic radii given in Fig. 9.1 (p.291). (3 points) b) Consider the formation of carbides (MC) of these metals. Which metal is able to accommodate carbon atoms better, and which cavities (octahedral or tetrahedral) would be better suited to accommodate C atoms into metal's lattice? (4 points)arrow_forward
- 2. Read paragraph 3.4 in your textbook ("Chiral Molecules"), and explain if Cobalt(ethylenediamine) 33+ shown in previous problem is a chiral species. If yes, draw projections of both enantiomers as mirror images, analogous to mirror projections of hands (below). Mirror (4 points)arrow_forward3. Borane (BH3) belongs to D3h point group. Consider the vibrational (stretching) modes possible for B-H bonds under D3h symmetry. Using the methods we used in class, construct the reducible representation I, and break it down into irreducible representations using the character table provided. Sketch those modes, indicate whether they are IR-active. (6 points) D3h E 2C3 3C2 σh 283 30% A₁' 1 1 1 1 1 1 x² + y², z² 1 -1 1 1 -1 R₂ E' 2 0 2 0 (x, y) (x² - y², xy) " A₁" 1 1 -1 A2" 1 -1 -1 1 Z E" 2 -1 0 -2 1 0 (Ry, Ry) (xz, yz)arrow_forward1. List all the symmetry elements, and assign the compounds to proper point groups: a) HCIBrC-BrCIH Cl Br H (2 points) H Br b) Pentacarbonylmanganese(I)bromide Br OEC-Mn-CEO 00- c) Phenazine (aromatic molecule, with delocalized bonding) 1 d) Cobalt(ethylenediamine)33+ (just the cation) 3+ H₂N H₂ .NH2 (CI)3 NH2 H2 H₂N. (2 points) (2 points) (2 points)arrow_forward
- Hello, I desperately need help figuring out 8-14; I also wanted to see if you would mind letting me know if I picked the right degree as my melting points on the two graphs. Please and thank you in advance! All the information is provided.arrow_forwardThe reaction: A + B ⇌ 2 C, can be represented by the equilibrium expression, KC =[C]2[A][B]=258 at 520K.When 1.00 M of C was allowed to reach equilibrium and 0.055 M of A was formed. If this reaction wasperformed at the same temperature using 0.500 M C, what would the equilibrium concentration of Abe?arrow_forward1. What is the functional group of an alcohol and a phenol? 2. Why are some alcohols soluble in water? 3. Classify each of the following alcohols as primary, secondary or tertiary. a. 3-pentanol b. 2-methyl-2-butanol c. 1-propanolarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)