(a)
Interpretation:
The structural formula of 2,3-Dimethylcyclobutane should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Saturated hydrocarbon is known as
The compounds in which series of atoms are connected to form a ring is known as cyclic compound whereas the compounds which are open chain compounds and their atoms doesn't form a ring is known as acyclic compounds. The general molecular formula of cyclic alkane is
Rules of drawing structures of cycloalkanes are:
- First identify the base name, and then draw the cyclic ring of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(b)
Interpretation:
The structural formula of 2-Methyl-2-butene should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons.
Rules of drawing structures of
- First identify the base name, and then draw the straight chain of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(c)
Interpretation:
The structural formula of 2-Methyl-1,3-butadiene should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Unsaturated hydrocarbon having one or more double bond is known as alkene having general molecular formula
Rules of drawing structures of alkenes are:
- First identify the base name, and then draw the straight chain of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(d)
Interpretation:
The structural formula of 2,3-Dimethyl-3-ethylhexane should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Saturated hydrocarbon is known as alkane having general molecular formula
Rules of drawing structures of alkanes are:
- First identify the base name, and then draw the straight chain of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(e)
Interpretation:
The structural formula of 4,5-diethyloctane should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Saturated hydrocarbon is known as alkane having general molecular formula
Rules of drawing structures of alkanes are:
- First identify the base name, and then draw the straight chain of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(f)
Interpretation:
The structural formula of Cyclooctene should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Unsaturated hydrocarbon with one or more double bond is known as alkene having general molecular formula
The compounds in which series of atoms are connected to form a ring is known as cyclic compound whereas the compounds which are open chain compounds and their atoms doesn't form a ring is known as acyclic compounds. The general molecular formula of cyclic alkene is
Where, m represents number of double bonds.
Rules of drawing structures of cycloalkenes are:
- First identify the base name, and then draw the cyclic ring of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(g)
Interpretation:
The structural formula of Propadiene should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Unsaturated hydrocarbon having one or more double bond is known as alkene having general molecular formula
Rules of drawing structures of alkenes are:
- First identify the base name, and then draw the straight chain of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).
(h)
Interpretation:
The structural formula of 2-pentyne should be drawn.
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons. Unsaturated hydrocarbon with one or more triple bond is known as alkyne having general molecular formula
Rules of drawing structures of
- First identify the base name, and then draw the straight chain of carbon atoms according to the base name.
- After that according to the given position of the substituents, locate them on carbon atoms (replacement of hydrogen atom occurs).

Trending nowThis is a popular solution!

Chapter 7 Solutions
OWLV2 FOR OXTOBY/GILLIS/BUTLER'S PRINCI
- Normalized Intensity (a. u.) 0.5 1.0 A 3D-printed GC column (shown below) was created for use with "micro" gas chromatography applications. To prove its utility, it was used to separate a mixture of alkanes (C9-C18, C22, C24). For the separation shown below, the column temperature was ramped from 40 °C to 250 °C at a rate of 30 °C per minute. (a) 9 10 = 1 mm 12 13 15 22 0.0 0 100 200 300 400 Time (sec) a) What detector would you use for this analysis? Justify your selection. b) Explain how the chromatogram would change if the separation was run isothermally. c) Explain how the chromatogram would change if the temperature ramp were increased to 50 °C per minute.arrow_forwardDevise a synthesis of each compound from the indicated starting material. You may also use any organic compounds with one or two carbons and any needed inorganic reagents. a. Brarrow_forwardPlease help me with #2b & #3 using the data.arrow_forward
- Heparin is used as an anti-coagulant. A risk of heparin use is thrombocytopenia, or low platelet count. This risk is minimized with the use of low molecular weight heparins (LMWH), therefore it is desirable to separate LMWH from higher molecular weight heparins. The method of choice to do this is molecular exclusion chromatography. Below is a chromatogram from a molecular exclusion chromatographic run. Peaks ranging from A to J are clearly distinguishable. The heparin mixture that was analyzed had anywhere from 6 to 30 repeat units of monomer (where the heparin with 30 repeat units would be roughly five times the size of the heparin with six repeat units). a. Which letter most likely represents the peak with 6 repeat units given these heparin polymers were separated with molecular exclusion chromatography? b. Explain your reasoning describing the mechanism of retention in molecular exclusion chromatography. 100 80 60 60 Relative Abundance 40 40 E GH 20 20 B A 36 38 40 42 44 46 48 50 50…arrow_forwardHELP NOW PLEASE ! URGENT!arrow_forwardHELP NOW PLEASE ! URGENT!arrow_forward
- Draw a Newman projection for the molecule below from the perspective indicated. Which of the groups (letters A-H) are methyl groups? CH3 H H H A H B ☑ >> H. ABCDEFG I H -H CH3 G D CH F E Numeric 4 points How many gauche interactions exist in the conformation shown in the previous problem? 1arrow_forwardHELP NOW PLEASE ! ASAP! URGENT!arrow_forwardHELP NOW PLEASE ! ASAP! URGENT!arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningWorld of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College Div




