Concept explainers
(a)
Interpretation:
The structure of the given compound (2,3-dimethyloctane) 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
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 (1-ethyl-3-methylcyclohexane) 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
(c)
Interpretation:
The name of the given compound has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. The general formula for alkanes can be given as
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
(d)
Interpretation:
The name of the given compound has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. The general formula for alkanes can be given as
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
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Chapter 15 Solutions
CHEMISTRY MOLECULAR NATURE OF MATTER
- Nonearrow_forward(9 Pts) In one of the two Rare Earth element rows of the periodic table, identify an exception to the general ionization energy (IE) trend. For the two elements involved, answer the following questions. Be sure to cite sources for all physical data that you use. a. (2 pts) Identify the two elements and write their electronic configurations. b. (2 pts) Based on their configurations, propose a reason for the IE trend exception. c. (5 pts) Calculate effective nuclear charges for the last electron in each element and the Allred-Rochow electronegativity values for the two elements. Can any of these values explain the IE trend exception? Explain how (not) - include a description of how IE relates to electronegativity.arrow_forwardPlease explain thoroughly and provide steps to draw.arrow_forward
- As you can see in the picture, the instrument uses a Xe source. Given that the instrument is capable of measuring from 200-800nm, if Xe was not used, what other source(s) could be used? Refer to figure 7-3. How many monochrometers does this instrument have? Why? Trace the light as it goes from the Xenon lamp all the way to the circle just slightly to the right and a little bit down from S4. What do you think that circle is? In class we talked about many types of these, which kind do you think this one is for a fluorimeter? Why? Explain. What is/are some strategy(ies) that this instrument has for dealing with noise that you see present in the optics diagram? Why does a fluorescence cuvette have to be clear on four sides?arrow_forwardProvide steps and thoroughly solve.arrow_forwardNonearrow_forward
- Devise a synthesis to prepare 4-tert-butyl-2-nitrotoluene from toluene. Complete the following reaction scheme. Part 1 of 4 Step 1 Step 2 A B Draw the structure for compound B, 4-tert-butyl-2-nitrotoluene. Click and drag to start drawing a structure. 'O Х ப:arrow_forwardWhat is N hybridized? sp3 or sp2? whyarrow_forwardDate Unknown o Hydrated Salt Lab Sec. Name Trial I Trial 2 1. Mass of fired crucible and lid (g) 2. Mass of fired crucible, lid, and hydrated sah (g) 3. Instructor's approval of flame and apparatus 4. Mass of crucible, lid, and anhydrous salt Ist mass measurement (g) 2nd mass measurement (g) 3rd mass measurement (g). Desk No. Trial 3 48.833 46.808 213.692 51.507 9.359 46,615 50.296 48.211 45.351 50.142 48.146 45.1911 50.103 48.132 45.186 5. Final mass of crucible, lid, and anhydrous salt (g) 50.180 4.13 45.243 Calculations 1. Mass of hydrated salt (g) 2. Mass of anhydrous salt (g) 2.674 2.491 2.9239 1.3479 1.2959 1.5519 3. Mass of water lost (g) 1.32791969 1.322g 4. Percent by mass of volatile water in hydrated salt (%) 49.6% 48% 216.9% 5. Average percent HO in bydrated salt (%H,O) 5. Standard deviation of %H,O Relative standard deviation of %H,O in hydrated salt (RSD) how calculations on next page. 48.17% Data Analysis, B Data Analysis, C Data Analysis, D Experiment 5 89arrow_forward
- Considering the irregular electronic configurations we discussed for certain transitionmetals, think about the possibility of silicon (Si) having a [Ne]3s 2 3p 2 configuration vs.[Ne]3s 1 3p 3. Discuss the pros and cons of both configurations. Which one does Si actuallyadopt and why?arrow_forward(5 Pts) Currently, the last element in the periodic table is number 118, oganesson (Og). Channel your inner Dimitri Mendeleev and predict element 119’s electronic configuration, atomic mass, density, and either melting or boiling point. Justify your answers.arrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
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