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What else can I help you with?
Is CH single bond or double bond?
CH compound does not exist. So it has no bonds.
Calculate the number of molecules in 8.0 moles of CH?
CH is not a molecule.
Can you calculate the number of molecules in 8.0 moles of CH?
CH is not a molecule.
What are Bis-allylic protons?
Bis allylic protons are nuclei of hydrogen atoms (bonded to the same carbon atom) that are in allylic positions with respect to two different C=C double-bonds. For example, the bolded hydrogen atoms in the structure below represent bis allylic protons, since they are in an allylic position with respect to the C=C bonds on both the left and the right.R-CH=CH-CH2-CH=CH-R
What are the differences between saturated unsaturated mono saturated and polyunsaturated fatty acids?
Fats are a type of triglyceride. This is aglycerol ( H-CHOH-CHOH-CHOH-H ) molecule reacted with three fatty acids. ( R-COOH ) where R is a long chain carbon molecule. In this chain there can be single carbon carbon bonds or double carbon carbon bonds. A saturated fat is one where all bonds are single. A monounsaturated fat contains a single carbon carbon double bond. A polyunsaturated fat has more than one. If R is H-CH2-CH2-CH2-CH2-CO-O-G it is a saturated fat. If it is H-CH2-CH2-CH=CH-CO-O-G it is monounsaturated. If it is H-CH=CH-CH=CH-CO-O-G then it has two and therefore polyunsaturated. The G stands for glycerol (Sometimes glycerine) .
What are CH and OH bonds?
Ch and OH bonds are covalent in nature. Ch bond is non -polar while OH bond is polar covalent bond.
Is CH single bond or double bond?
CH compound does not exist. So it has no bonds.
What is cross conjugation?
Cross-conjugation is a special type of conjugation in a molecule, when in a set of three Pi bonds only two pi-bonds interact with each other by conjugation, the third one is excluded from interaction [1]. In classical terms it means that the strict alternation of single and double bonds --CH=CH–CH=CH–CH-- (i.e., conjugated) is interrupted by two consecutive single bonds at each cross-conjugated point in the cross-conjugated pathway: --CH=CH–C(=CH)–CH=CH--. Examples of cross-conjugation can be found in molecules such as benzophenone, divinylether, dendralenes and fullerene. The type of conjugation has an impact on reactivity and molecular electronic transitions.
CH 3 - CH 2- CH 2- CH 3 - CH 2- CH 2- CH 3?
This is a chain of seven carbon atoms with alternating single bonds. The molecule is an alkane, specifically heptane. It is a straight-chain hydrocarbon commonly used as a fuel in gasoline.
What type of bond is in a lipid?
Nonpolar CH bonds. Ester linkages occur.
What is angle between ch bond in alkane?
The bond angle between two CH bonds in an alkane is approximately 109.5 degrees. This is because the bonds are arranged tetrahedrally around the carbon atom, resulting in a bond angle of 109.5 degrees.
Calculate the number of molecules in 8.0 moles of CH?
CH is not a molecule.
Can you calculate the number of molecules in 8.0 moles of CH?
CH is not a molecule.
What are Bis-allylic protons?
Bis allylic protons are nuclei of hydrogen atoms (bonded to the same carbon atom) that are in allylic positions with respect to two different C=C double-bonds. For example, the bolded hydrogen atoms in the structure below represent bis allylic protons, since they are in an allylic position with respect to the C=C bonds on both the left and the right.R-CH=CH-CH2-CH=CH-R
Which is the name of ch2 equals ch-ch equals ch2?
Those aren't equal signs, those are double bonds. When there are two double bonds in a compound, it has the suffix: -diene. So, we have 4 carbons, which means it's a but-, and 6 Hydrogens. So the formula is C4H6: 1,3-butadiene
Equation for reaction of bromine with cooking oil?
Cooking oils are unsaturated triglycerides so Bromine add up on pi bonds, R-CH=CH-(CH2)n-COOR + Br2 = R-CH(Br)-CH(Br)-(CH2)n-COOR , the confirmation of reaction is the decolourisation of Bromine.
What are bis allylic protons?
Bis allylic protons refer to protons that are adjacent to two allylic carbons in a molecule. They are typically more deshielded and can show unique chemical shifts in the NMR spectrum due to their proximity to multiple double bonds.
