Seven elements make up the compound
Answer:
The correct answer is hydrolysis of poly saccharides
Explanation:
Polysaccharides are composed of numerous monosaccharides units joined with each other by glycosidic linkages.If the polysaccharides are treated with strong acids such as Hydrochloric acid or hydrolytic the glycosidic linkages are broken down resulting in the formation of monosaccharide constituents.
For example homo polysaccharide plant poly saccharide starch is composed of glucose units linked with one another by α-1,4-glycosidic linkage.When starch is digested by amylase enzyme then hydrolysis of starch occur resulting in the formation of di saccharide maltose, dextrin and maltitriose which further undergo hydrolysis by the catalytic activity of various hydrolytic enzymes to generate momosaccharide sububits.
Explanation:
Answer:
when the sun's light hits a living thing
Answer:
The three ways to in which the hydrocarbons are represented are;
a. The ball and stick model
b. Condensed structural formula
c. Skeletal structure
The molecular formula are
a. C₇H₁₆
b. C₆H₁₄
c. C₅H₁₂
Explanation:
a. The ball and stick model of organic compounds, displays the atoms and bonds in three dimensions, representing the atoms by spares and the bonds by rods
b. The condensed structural formula are similar to the structural formula with the difference that the formula is written in a linear fashion which conserves space and increases ease of writing and are written out faster.
c. In the skeletal structure diagram, the atoms are of the organic compound are combined together in the structural drawing of the essential features of the organic compound. In essence, a skeletal structure, depicts the skeleton of a compound as it is made up of the molecule's skeletal atoms.
Answer:
See explanation
Explanation:
It is clear that certain substituted benzene compounds reacts faster than benzene during electrophillic substitution reactions. This owes to the activation of the benzene ring towards electrophillic substitution by resonance.
The -OCH3 group is ortho- para directing hence it directs an incoming electrophile (such as during bromination) to the ortho or para position as shown in the image attached. This occurs due to resonance (mesomeric) effect as shown in the image attached to this answer.
Image credit: pinterest