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Melting Temperature Hydrocarbons Alkane Alkene Benzene Aromatic Alcohol Acid Naphthalene

Reference data and engineering information about melting temperature hydrocarbons alkane alkene benzene aromatic alcohol acid naphthalene for thermodynamics applications.

meltingtemperaturehydrocarbonsalkane

Overview

Engineering reference data for Melting Temperature Hydrocarbons Alkane Alkene Benzene Aromatic Alcohol Acid Naphthalene in thermodynamics.

Key Formulas

First Law

ΔU=QW\Delta U = Q - W

Energy is conserved — heat added minus work done.

Ideal Gas Law

PV=nRTPV = nRT

Relates pressure, volume, and temperature of an ideal gas.

Heat Transfer

Q=mcΔTQ = mc\Delta T

Sensible heat transfer.

Carnot Efficiency

η=1TC/TH\eta = 1 - T_C/T_H

Maximum efficiency between two temperatures.

Variables

SymbolDescriptionUnit
UUInternal energyJ
QQHeatJ
WWWorkJ
PPPressurePa
VVVolume
TTTemperatureK

Melting Point Data

7 rows
Melting points of hydrocarbons, alcohols, and acids (C7–C16) in °C
Compound Type
C7(°C)
C8(°C)
C9(°C)
C10(°C)
C11(°C)
C12(°C)
C13(°C)
C14(°C)
C15(°C)
C16(°C)
n-Alkane-91-57-53-30-26-10
1-Alkene-119-102-81-66-49-35-23-13-44
Alkylbenzene-63-48-36-24-14
1-Alkanol-33-15-571724313844
Alkanoic acid-717123129444263
Alkylcyclohexane-48-31-20-10-2
2-Methylalkane-80-75-49-47

Source: engineeringtoolbox.com

Compound Definitions

CompoundFormulaDescription
AlkaneCnH2n+2C_nH_{2n+2}Acyclic saturated hydrocarbon (paraffin)
AlkeneCnH2nC_nH_{2n}Unsaturated hydrocarbon with at least one C=C double bond (olefin)
AlkyneCnH2n2C_nH_{2n-2}Unsaturated hydrocarbon with at least one C≡C triple bond (acetylene)
CycloalkaneCnH2nC_nH_{2n}Monocyclic saturated hydrocarbon (naphthene)
CycloalkeneCnH2n2C_nH_{2n-2}Alkene with a closed ring, non-aromatic (cycloolefin)
BenzeneC6H6C_6H_6Simplest aromatic hydrocarbon, one ring
NaphthaleneC10H8C_{10}H_8Two-ring aromatic hydrocarbon
Alkyl groupCnH2n+1C_nH_{2n+1}Alkane substituent missing one hydrogen

For hydrocarbons with the same carbon number, boiling points increase in this order:

multisubstituted alkane<single-substituted alkane<single-substituted alkene<normal alkene<normal alkane\text{multisubstituted alkane} < \text{single-substituted alkane} < \text{single-substituted alkene} < \text{normal alkene} < \text{normal alkane}

<alkyl cyclohexane<alkylbenzene<cycloalkene<cycloalkane< \text{alkyl cyclohexane} < \text{alkylbenzene} < \text{cycloalkene} < \text{cycloalkane}

<2-, 4-, 3-alkanol / 1-alkylnaphthalene<1-alkanol<normal alkanoic acid< \text{2-, 4-, 3-alkanol / 1-alkylnaphthalene} < \text{1-alkanol} < \text{normal alkanoic acid}

Note: Melting point trends are more variable with increasing carbon number compared to boiling points, as molecular symmetry and crystal packing efficiency significantly influence solid-phase transitions.

Interactive Charts

Melting point figure

References