![card image](../uploads/185/14/20d22d11_17eb643ad47__8000_00003840.png)
Give the IUPAC name for the following compound
1-sec-butyl-4-isopropyl-2-methylcyclohexane
![card image](../uploads/186/15/20d22d11_17eb643ad47__8000_00003866.png)
Give the IUPAC name for the following compound
3,5-diethyl-2-methylheptane
![card image](../uploads/187/16/20d22d11_17eb643ad47__8000_00003868.png)
Give the IUPAC name for the following compound
1-cyclopentylhexane
Draw an appropriate structure given the IUPAC name of the following compound:
5-sec-butyl-3-ethyl-2,7-dimethyldecane
![card image](../uploads/188/17/20d22d11_17eb643ad47__8000_00003844.png)
Draw an appropriate structure given the IUPAC name of the following compound:
4-ethyl-3,6-dimethyloctane
![card image](../uploads/189/18/20d22d11_17eb643ad47__8000_00003870.png)
![card image](../uploads/190/19/20d22d11_17eb643ad47__8000_00003836.png)
Convert the following structure to a Newman Projection. Rotate projection 60 degrees and identify which conformation is more stable.
![card image](../uploads/191/20/20d22d11_17eb643ad47__8000_00003838.png)
**The rotated conformation is neither the most or least stable. The least stable would have the methyl groups eclipsing each other.
![card image](../uploads/192/21/20d22d11_17eb643ad47__8000_00003862.png)
Convert the following structure to a Newman Projection (The eye is on the lefthand side). Rotate projection 60 degrees and identify which conformation is higher in energy.
![card image](../uploads/193/22/20d22d11_17eb643ad47__8000_00003864.png)
![card image](../uploads/194/23/20d22d11_17eb643ad47__8000_00003854.png)
Classify the following reaction as oxidation, reduction, or neither.
Neither
![card image](../uploads/195/24/20d22d11_17eb643ad47__8000_00003852.png)
Classify the following reaction as oxidation, reduction, or neither.
Oxidation
![card image](../uploads/196/25/20d22d11_17eb643ad47__8000_00003846.png)
Draw another conformer of the structure provided of cis-cyclohexane-1,3-diol. Identify which is most stable.
![card image](../uploads/1195/34/20d22d11_17eb643ad47__8000_00006052.png)
The conformer following the ring flip is more stable because the substituents (large groups) are avoiding 1,3-trans-diaxial interactions.
Draw an appropriate conformer for cis-1-ethyl-3-isopropylcyclohexane. Perform a ring flip, and then determine which is the least stable conformation.
![card image](../uploads/198/27/20d22d11_17eb643ad47__8000_00003850.png)
![card image](../uploads/199/28/20d22d11_17eb643ad47__8000_00003858.png)
Draw a possible chair conformation for the substituted cyclohexane
![card image](../uploads/200/29/20d22d11_17eb643ad47__8000_00003860.png)
![card image](../uploads/201/30/20d22d11_17eb643ad47__8000_00003872.png)
Draw a possible chair conformation for the substituted cyclohexane
![card image](../uploads/202/31/20d22d11_17eb643ad47__8000_00003874.png)