This is too much and too complicated to calculate:
There are many possibilities for 1 or more double, triple, linear, branched or cyclic CC-bonds with one C=O or C-OH group on many different C-atoms.
One reasonable possibility is: 2,4,6-hepta-tri-enal, H2C=CH-CH=CH-CH=CH-CH(=O)
The answer would give no interesting views on organic structural chemistry.
But maybe C3H8O is meant (C3.. in stead of C7..), this will give you only two possible isomers: 1-propanol and 2-propanol.
Structural isomers also called constitutional isomers are different compounds that have same molecular formula but different molecular structure. Structural isomers have same number of each type of atoms but the atoms are connected in a different order in them. Structural isomerism is seen in organic compounds. It can be due to different arrangement of carbon chain, due to different position of functional group on the carbon chain, due to different functional groups that give their family of compounds same molecular formula. Difference in arrangement of atoms is visible if structural formulas are written for compounds having same molecular formula. Like structural isomers, stereoisomers also have same molecular formula. Stereoisomers are not structural isomers. Stereoisomers have their atoms connected in same sequence( same constitution), but they differ in the arrangement of atoms in space. Cis and trans isomers of alkenes are examples of stereoisomers. Carbon chain arrangement, position of functional groups, and everything that could be different in structural isomerism is same here.
Lithium oxide does not exist as molecules, as it is an ionic compound.
In chemistry, isomers (from Greek ισομερης, isomerès; isos = "equal", méros = "part") are compounds with the same molecular formula but different structural formulas. Isomers do not necessarily share similar properties, unless they also have the same functional groups. There are many different classes of isomers, like stereoisomers, enantiomers, geometrical isomers, etc. (see chart below). There are two[citation needed] main forms of isomerism: structural isomerism and stereoisomerism (spatial isomerism).
Diacetylferrocene can have three possible isomers: symmetrical cis-diacetylferrocene, symmetrical trans-diacetylferrocene, and unsymmetrical diacetylferrocene.
There are three isomers of C2H2Br2: 1,1-dibromoethane, 1,2-dibromoethane, and vinyl bromide.
An isomer is a molecule or compound that has the same number of atoms as another but a different structure, different physical and chemical properties. Isomers can exist because in large molecules there are several different ways you can position the same elements to make different structures.
Structural isomers also called constitutional isomers are different compounds that have same molecular formula but different molecular structure. Structural isomers have same number of each type of atoms but the atoms are connected in a different order in them. Structural isomerism is seen in organic compounds. It can be due to different arrangement of carbon chain, due to different position of functional group on the carbon chain, due to different functional groups that give their family of compounds same molecular formula. Difference in arrangement of atoms is visible if structural formulas are written for compounds having same molecular formula. Like structural isomers, stereoisomers also have same molecular formula. Stereoisomers are not structural isomers. Stereoisomers have their atoms connected in same sequence( same constitution), but they differ in the arrangement of atoms in space. Cis and trans isomers of alkenes are examples of stereoisomers. Carbon chain arrangement, position of functional groups, and everything that could be different in structural isomerism is same here.
Lithium oxide does not exist as molecules, as it is an ionic compound.
Molecular compounds are not always written in their lowest ratio because the ratio may not simplify further without changing the identity of the compound. Additionally, different ratios can exist due to isomers, which are compounds with the same molecular formula but different structural arrangements.
In chemistry, isomers (from Greek ισομερης, isomerès; isos = "equal", méros = "part") are compounds with the same molecular formula but different structural formulas. Isomers do not necessarily share similar properties, unless they also have the same functional groups. There are many different classes of isomers, like stereoisomers, enantiomers, geometrical isomers, etc. (see chart below). There are two[citation needed] main forms of isomerism: structural isomerism and stereoisomerism (spatial isomerism).
Fiber food is not a compound and a chemical formula doesn't exist.
Yes.
Butune is a nonsubstituted alkane that can exist as one of only two isomers.
Diacetylferrocene can have three possible isomers: symmetrical cis-diacetylferrocene, symmetrical trans-diacetylferrocene, and unsymmetrical diacetylferrocene.
Not quite. Isomers are compounds that have the same molecular formula but different structures. In general, a molecule will not spontaneously convert from one isomer to another. Tautomers are a specific type of isomers. Two molecules are tautomers if they differ in the placement of a proton (H+) and a double bond, and readily convert between the two, creating an equilibrium. For example, one common type of tautomerism is between an enol and a ketone (or aldehyde). In this case, the keto form contains a carbon double-bonded to an oxygen adjacent to a carbon with at least one hydrogen. This is in equilibrium with the enol, which is formed by moving a hydrogen from the second carbon to the oxygen (forming -OH) and the double bond to the oxygen is broken and reformed between the two carbons.
Well let me see... isomers are compounds which share the same moecular formula (ieC6H14) but have different structures. So isomers of hexane (c6h14) include: Hexane 2-Methylpentane 3-Methylpentane 2,3-Dimethylbutane 2,2-Dimethylbutane Hope this helps
There are three isomers of C2H2Br2: 1,1-dibromoethane, 1,2-dibromoethane, and vinyl bromide.