(a)
Interpretation:
The systematic name for the below given compound has to be given.
Concept Introduction:
The hydrocarbons which contains 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 systematic name for the below given compound has to be given.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. When alkane loses two hydrogens and forms a cyclic ring, it is said to be cycloalkane. The general formula for cycloalkanes can be given as
The Alkanes are named following some rules:
- The name of the cycloalkane is given by the number of carbon atoms present in the ring. It is said to be Root of the cycloalkane.
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 ring 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 ring.
- The name of the cycloalkane is given in the form
Prefix + Root + Suffix
(c)
Interpretation:
The systematic name for the given compound has to be given and the geometric isomer present in the compound has to be identified.
Concept Introduction:
The hydrocarbons which contains double bonds are said to be
The Alkenes are named following some rules:
- The name of the alkene is given by the number of carbon atoms including the double bonded carbon atoms in the chain. It is said to be Root of the alkene.
Root = number of carbon atoms in chain including the double bond.
- 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 ring 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 ring.
- The name of the cycloalkane is given in the form
Prefix + Root + Suffix
The geometrical isomers have different orientations of groups around a double bond. The geometric isomers are cis-trans isomers. The isomer which contains same groups or equally prioritized groups on the same side of the double bonded carbon atoms, it is said to be cis-isomer. If the same groups or equally prioritized groups are present on the opposite sides of the double bonded carbon atoms, it is said to be trans-isomer.
(d)
Interpretation:
The systematic name for the given compound has to be given and the chiral centers has to be identified.
Concept Introduction:
The hydrocarbons which contains only single bonds are said to be Alkanes. When alkane loses two hydrogens and forms a cyclic ring, it is said to be cycloalkane. The general formula for cycloalkanes can be given as
The Alkanes are named following some rules:
- The name of the cycloalkane is given by the number of carbon atoms present in the ring. It is said to be Root of the cycloalkane.
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 ring 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 ring.
- The name of the cycloalkane is given in the form
Prefix + Root + Suffix
The atom is said to be as chiral when it is attached to four different groups. It is asymmetrical and does not super-impose on its mirror image. In a compound, the atom which is asymmetric is chiral and is called chiral centre.
Want to see the full answer?
Check out a sample textbook solutionChapter 15 Solutions
Loose Leaf for Chemistry: The Molecular Nature of Matter and Change
- 1) Suppose 0.1 kg ice at 0°C (273K) is in 0.5kg water at 20°C (293K). What is the change in entropy of the ice as it melts at 0°? To produce the original "water gas" mixture, carbon (in a combustible form known as coke) is reacted with steam: 131.4 kJ + H20(g) + C(s) → CO(g) + H2(g) From this information and the equations in the previous problem, calculate the enthalpy for the combustion or carbon to form carbon dioxide. kindly show me how to solve both parts of the same long problem. Thanksarrow_forwardwe were assigned to dilute 900ppm in to 18ppm by using only 250ml vol flask. firstly we did calc and convert 900ppm to 0.9 ppm to dilute in 1 liter. to begin the experiment we took 0,225g of kmno4 and dissolved in to 250 vol flask. then further we took 10 ml sample sol and dissolved in to 100 ml vol flask and put it in to a spectrometer and got value of 0.145A . upon further calc we got v2 as 50ml . need to find DF, % error (expval and accptVal), molarity, molality. please write the whole report. thank you The format, tables, introduction, procedure and observation, result, calculations, discussion and conclusionarrow_forwardQ5. Predict the organic product(s) for the following transformations. If no reaction will take place (or the reaction is not synthetically useful), write "N.R.". Determine what type of transition state is present for each reaction (think Hammond Postulate). I Br₂ CH3 F2, light CH3 Heat CH3 F₂ Heat Br2, light 12, light CH3 Cl2, light Noarrow_forward
- Nonearrow_forwardIn the phase diagram of steel (two components Fe and C), region A is the gamma austenite solid and region B contains the gamma solid and liquid. Indicate the degrees of freedom that the fields A and B have,arrow_forwardFor a condensed binary system in equilibrium at constant pressure, indicate the maximum number of phases that can exist.arrow_forward
- Part V. Label ad match the carbons in compounds Jane and Diane w/ the corresponding peak no. in the Spectra (Note: use the given peak no. To label the carbons, other peak no are intentionally omitted) 7 4 2 -0.13 -0.12 -0.11 -0.10 -0.08 8 CI Jane 1 -0.09 5 210 200 190 180 170 160 150 140 130 120 110 100 -8 90 f1 (ppm) 11 8 172.4 172.0 f1 (ppr HO CI NH Diane 7 3 11 80 80 -80 -R 70 60 60 2 5 -8 50 40 8. 170 160 150 140 130 120 110 100 90 -0 80 70 20 f1 (ppm) 15 30 -20 20 -60 60 -0.07 -0.06 -0.05 -0.04 -0.03 -0.02 -0.01 -0.00 -0.01 10 -0.17 16 15 56 16 -0.16 -0.15 -0.14 -0.13 -0.12 -0.11 -0.10 -0.09 -0.08 -0.07 -0.06 -0.05 -0.04 17.8 17.6 17.4 17.2 17.0 f1 (ppm) -0.03 -0.02 550 106 40 30 20 20 -0.01 -0.00 F-0.01 10 0arrow_forwardConsider the reaction of 2-methylpropane with a halogen. With which halogen will the product be almost exclusively 2-halo-2-methylpropane? 1. F2 2. Cl2 3. Br2 4. I2arrow_forwardNonearrow_forward
- Nonearrow_forwardn Feb 3 A T + 4. (2 pts) Draw the structure of the major component of the Limonene isolated. Explain how you confirmed the structure. 5. (2 pts) Draw the fragment corresponding to the base peak in the Mass spectrum of Limonene. 6. (1 pts) Predict the 1H NMR spectral data of R-Limonene. Proton NMR: 5.3 pon multiplet (H Ringarrow_forwardPart VI. Ca H 10 O is the molecular formula of compound Tom and gives the in the table below. Give a possible structure for compound Tom. 13C Signals summarized C1 C2 C3 C4 C5 C6 C7 13C shift (ppm) 23.5 27.0 33.0 35.8 127 162 205 DEPT-90 + DEPT-135 + +arrow_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