Classify the following hydrocarbons, and draw a Lewis structure for each one. A compound may fit into more than one of the following classifications:
alkane
alkene
alkyne
cycloalkane
cycloalkene
cycloalkyne
aromatic
hydrocarbon
(g)
(h)
(i)

Verified step by step guidance

1. Step 1: Begin by identifying the general formula for each type of hydrocarbon. Alkanes have the formula CnH2n+2, alkenes CnH2n, alkynes CnH2n-2, cycloalkanes CnH2n, cycloalkenes CnH2n-2, cycloalkynes CnH2n-4, and aromatic hydrocarbons typically follow the formula CnHn.
2. Step 2: Analyze the molecular formula of each compound (g, h, i) to determine which category or categories they fit into. Compare the number of carbon and hydrogen atoms to the general formulas identified in Step 1.
3. Step 3: Consider structural features such as rings or double/triple bonds. Cycloalkanes, cycloalkenes, and cycloalkynes contain rings, while alkenes and alkynes contain double and triple bonds respectively. Aromatic hydrocarbons have a distinct ring structure with alternating double bonds.
4. Step 4: Draw the Lewis structure for each compound. Start by arranging the carbon atoms in the appropriate structure (linear, cyclic, etc.), then add hydrogen atoms to satisfy the valency of carbon (four bonds per carbon atom). Ensure that double or triple bonds are correctly represented where applicable.
5. Step 5: Verify the classification by checking the drawn Lewis structure against the characteristics of each hydrocarbon type. Ensure that the structure adheres to the rules of organic chemistry, such as the octet rule for carbon and hydrogen.

Key Concepts

Hydrocarbon Classification

Hydrocarbons are organic compounds consisting entirely of hydrogen and carbon. They are classified based on the types of bonds between carbon atoms: alkanes have single bonds, alkenes have at least one double bond, and alkynes have at least one triple bond. Cyclic hydrocarbons form rings, and aromatic hydrocarbons contain conjugated pi electron systems, typically in a ring structure like benzene.

Lewis Structures

Lewis structures are diagrams that represent the bonding between atoms of a molecule and the lone pairs of electrons that may exist. They are essential for visualizing the arrangement of atoms and the distribution of electrons in a molecule, helping to predict molecular geometry, reactivity, and polarity. Each line represents a bond, and dots represent lone electrons.

Aromaticity

Aromatic hydrocarbons are a special class of cyclic compounds characterized by stability due to resonance. They follow Huckel's rule, which states that a molecule is aromatic if it has a planar ring structure with (4n+2) pi electrons, where n is a non-negative integer. This delocalization of electrons results in unique chemical properties, such as increased stability and distinctive reactivity patterns.