Draw the structure of the acyclic alkane(s) that have 6 or fewer carbons and 2 tertiary hydrogens.
Draw the structure of the acyclic alkane(s) that have 6 or fewer carbons and 2 tertiary...
Draw the structure of the acyclic alkane(s) that have 8 carbons and only primary hydrogens. You do not have to consider stereochemistry. If more than one structure fits the description, draw them all. Draw one structure per sketcher. Add additional sketchers using the dropdown menu in the bottom right comer. Separate structures with + signs from the dropdown menu.
Draw the structure of an alkane that has 6 or fewer carbons, 1 of which is secondary and 1 of which is tertiary
Draw the structure of an alkane that has 5 or fewer carbons and 9 primary hydrogens.
Draw the structure(s) of all alkane(s) that have 7 carbons, 2 of which are tertiary. You do not have to consider stereochemistry. If more than one structure fits the description, draw them all. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate structures with + signs from the drop-down menu.
Draw the structure of an alkane that has 3-6 carbons and does not have secondary or tertiary carbons.
1. Draw the structure of an alkane or cycloalkane that has more than three but fewer than 9 carbon atoms and only primary hydrogens.B. Draw the structure of an alkane or cycloalkane that has 5 carbon atoms and only secondary Hydrogen atoms.
Draw the structure of an alkane or cycloalkane that has more than three but fewer than ten carbon atoms, and only primary hydrogens. (There are several possible structures. It is enough to draw any one of them, but you may draw two or more if you want to.)
I If you have an alkane and an alkenes with the same number of carbons (and no rings), what is the relationship between the number of hydrogens present on the two molecules, i.e., how do the molecular formulas differ? If you have an alcohol and an aldehyde (or ketone) with the same number of carbons (and no rings), what is the relationship between the number of hydrogens present on the two molecules, i.e., how do the molecular formulas differ? If...
Identify the molecule being described in the following statements. Unknown X is an acyclic 5-carbon alkane containing an alcohol functional group. Oxidation with PCC provides an aldehyde product. Dehydration with POCla/Pyridine gives a di-substituted alkene product. Provide a plausible structure for unknown X Unknown X is an acyclic 6-carbon alkane containing an alcohol with formula CsH13BrO. Treatment witlh NaH generates an unsymmetrical epoxide, which when treated with HBr generates a tertiary alkyl halide. The starting material cannot be oxidized, however...
5. Use a condensed structure to provide your answer. Propose a structure for an acyclic alkane having the following spectrum. The results of the DEPT spectra are given following the signals. IU 8 C,H2 CH₃ CH3