Concept explainers
Interpretation:
Among the given statements concerning the
Concept Introduction:
Alkanes are linear chain saturated hydrocarbons. The reactivity of alkanes are very less. They can be heated for a very long time in strong acids and bases without any reaction. Even strong reducing and strong oxidizing agents have less effect on alkanes.
Alkanes are not completely inert. Two important reactions that alkanes undergo are combustion and halogenation.
Combustion reaction is the one where reaction occurs between substance and oxygen which proceeds with evolution of light and heat. Due to the heat produced when alkanes are made to undergo combustion with oxygen, it is used as fuel.
Halogenation is a chemical reaction between a substance and halogen. The product of halogenation reaction is that one or more halogens are incorporated into molecules of the substance. Halogenation of hydrocarbon gives hydrocarbon derivatives as product where halogen atoms are substituted instead of hydrogen atoms.
Halogenation reaction of alkane is an example of substitution reaction. This is a reaction where a part of reacting molecule replaces an atom or group of atoms in hydrocarbon or hydrocarbon derivative.
Cycloalkanes are also similar to those of alkanes. Cycloalkanes also undergo combustion and halogenation reaction.
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Chapter 1 Solutions
EBK ORGANIC AND BIOLOGICAL CHEMISTRY
- Denote the dipole for the indicated bonds in the following molecules. H3C ✓ CH3 B F-CCl 3 Br-Cl H3C Si(CH3)3 wwwwwww OH НО. HO HO OH vitamin C CH3arrow_forwardFor the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Η 1 D EN Select Draw Templates More C H D N Erasearrow_forwardQ9: Explain why compound I is protonated on O while compound II is protonated on N. NH2 NH2 I IIarrow_forward
- AN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forwardAN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forward(a) What is the hybridization of the carbon in the methyl cation (CH3*) and in the methyl anion (CH3¯)? (b) What is the approximate H-C-H bond angle in the methyl cation and in the methyl anion?arrow_forward
- Q8: Draw the resonance structures for the following molecule. Show the curved arrows (how you derive each resonance structure). Circle the major resonance contributor.arrow_forwardQ4: Draw the Lewis structures for the cyanate ion (OCN) and the fulminate ion (CNO). Draw all possible resonance structures for each. Determine which form for each is the major resonance contributor.arrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. CH3 N CH3 HÖ: H3C CI: ::arrow_forward
- Q3: Draw the Lewis structures for nitromethane (CH3NO2) and methyl nitrite (CH3ONO). Draw at least two resonance forms for each. Determine which form for each is the major resonance contributor.arrow_forwardQ1: Draw a valid Lewis structures for the following molecules. Include appropriate charges and lone pair electrons. If there is more than one Lewis structure available, draw the best structure. NH3 Sulfate Boron tetrahydride. C3H8 (linear isomer) OCN NO3 CH3CN SO2Cl2 CH3OH2*arrow_forwardQ2: Draw all applicable resonance forms for the acetate ion CH3COO. Clearly show all lone pairs, charges, and arrow formalism.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