Just check for how many carbon groups are attached to the carbon group that OH is on. Since OH can only bond to one carbon, you see how many other carbons are attached to that one. The maximum is 3, since carbon usually only has 4 bonds total, making it tertiary structure. Likewise, 2 carbon groups attached to that carbon makes it secondary, and one C group is primary. Just write out a diagram and it should be easy!
primary alcohols react the fastest, with secondary alcohols next and tertiary alcoholsnot reacting at all. This is because the mechanism of this reaction is Sn1 which is a substituion reaction that favors attack on less crowded molecules
Primary consumers are herbivores that eat plants directly. Secondary consumers are carnivores that eat primary consumers. Tertiary consumers are carnivores that eat secondary consumers.
Yellow (primary color) Yellow-Green (tertiary color) Green (secondary color) Blue-Green (tertiary color) Blue (primary color) Blue-Purple (tertiary color) Purple (secondary color) Red-Purple (tertiary color) Red (primary color) Orange-Red (tertiary color) Orange (secondary color) Yellow-Orange (tertiary color) (and then you are back at yellow)
Primary alcohols are more resistant to oxidation compared to secondary and tertiary alcohols. This is because primary alcohols have a hydrogen atom attached to the carbon with the hydroxyl group, which can be oxidized to form an aldehyde or carboxylic acid.
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
it is a secondary alcohol
tertiary
primary 3% secondary 17% tertiary 80%
Secondary and tertiary
primary alcohols react the fastest, with secondary alcohols next and tertiary alcoholsnot reacting at all. This is because the mechanism of this reaction is Sn1 which is a substituion reaction that favors attack on less crowded molecules
Tertiary alcohols are more reactive towards oxidation with potassium permanganate compared to secondary alcohols. This is because the presence of more alkyl groups in tertiary alcohols stabilizes the intermediate carbocation formed during oxidation.
secondary
14% primary, 47% secondary, 28% tertiary and 11% Quatary
Primary: 33% Secondary: 15% Tertiary: 52% Same as Philipenis'
asda is secondary
secondary
tertiary