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Masteriza [31]
3 years ago
8

Consider the alkane below. Which property differentiates this alkane from other classes of alkanes?

Chemistry
2 answers:
maria [59]3 years ago
8 0

Answer is: A) The shape.

Name of this organic chemical compound is cyclohexane.

Cyclohexane is cycloalkane (the monocyclic saturated hydrocarbons).

Cyclohexane has single covalent bond and carbons have sp3 hybridization as other alkanes (for example propane).

Propane is alkane, organic compound. Carbons in propane have sp3 hybridization (carbon’s 2s and three 2p orbitals combine into four identical sp3 orbitals). Orbitals in sp3 hybridization have a tetrahedral arrangement and form single (sigma) bonds.

Elden [556K]3 years ago
5 0

Answer: Option (D) is the correct answer.

Explanation:

Alkanes are the hydrocarbons which contains only single bonds to join its corresponding atoms with each other.

In general, formula of an alkane is C_{n}H_{2n+2} where n is a whole number.

This general formula is applicable only for alkanes which are linear and branched in nature.

In linear alkane, atoms are attached in a chain like structure.And, in a branched alkane there will be presence of branches in the form of groupls like methyl, ethyl etc.

In cyclic alkanes, there will be single bonds between carbon and hydrogen atoms but the carbon atoms will bond together in the form of a ring. In a cyclic alkane, the number of hydrogen atoms will be less than the number of hydrogen atoms present in a linear or branched alkane.

So, in the given structure carbon atoms are attached to each other in the form of a ring. Hence, it is a cyclic alkane with less number of hydrogen atoms as compared to a linear alkane with a chain of 6 carbon atoms.

Thus, we can conclude that the number of hydrogen atoms is the property which differentiates this alkane from other classes of alkanes.

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3 years ago
How many moles of oxygen are present in 33.6l of the gas at 1atm and 0c
andreev551 [17]

The answer is: 1.5 moles of oxygen are present.

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5 0
3 years ago
A solution of 2-propanol and 1-octanol behaves ideally. Calculate the chemical potential of 2-propanol in solution relative to t
andrew-mc [135]

Answer:

The chemical potential of 2-propanol in solution relative to that of pure 2-propanol is lower by 2.63x10⁻³.    

Explanation:

The chemical potential of 2-propanol in solution relative to that of pure 2-propanol can be calculated using the following equation:

\mu (l) = \mu ^{\circ} (l) + R*T*ln(x)

<u>Where:</u>

<em>μ (l): is the chemical potential of 2-propanol in solution    </em>

<em>μ° (l): is the chemical potential of pure 2-propanol   </em>

<em>R: is the gas constant = 8.314 J K⁻¹ mol⁻¹ </em>

<em>T: is the temperature = 82.3 °C = 355.3 K </em>

<em>x: is the mole fraction of 2-propanol = 0.41 </em>

\mu (l) = \mu ^{\circ} (l) + 8.314 \frac{J}{K*mol}*355.3 K*ln(0.41)

\mu (l) = \mu ^{\circ} (l) - 2.63 \cdot 10^{3} J*mol^{-1}

\mu (l) - \mu ^{\circ} (l) = - 2.63 \cdot 10^{3} J*mol^{-1}  

Therefore, the chemical potential of 2-propanol in solution relative to that of pure 2-propanol is lower by 2.63x10⁻³.    

I hope it helps you!    

8 0
4 years ago
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