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Sophie Hanna Inglês 3 slides

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  1. Slide 1

    • Carbohydrates
    • -are hydrophilic organic molecules with the general formula
    • (CH2O)n. n=number of carbons.
    • - In the sugar glucose for example n=6 i.e. Glucose formula
    • =C6H12O6
    • - the names of most carbohydrates include the words
    • saccharide or ose both of which means sugar or sweet
    • The most well known carbohydrates are sugars, starch and
    • cellulose
    • Carbohydrates structure: they can be polyhydroxy aldehydes
    • or ketones or substances that can exist in a bonded form or as an open ring or
    • chain form as well
    • Carbohydrate classification:
    • carbohydrates are classified according to the number of units monosaccharides
    • (1 unit), disaccharides (2 units), oligosaccharides (>2-10 units),
    • polysaccharides (>10 units). 2) Functional groups represent aldehyde (-CHO),
    • ketone (-CO) 3) number of carbons within each unit (tri, tetra) 4) open ring or
    • chain form
  2. Slide 2

    • Monosaccharides: the simplest
    • carbohydrates also called simple sugars. They cannot be hydrolysed into smaller
    • units. Two groups aldoses (aldehyde group) e.g. Glucose, ketoses (ketone group)
    • e.g. fructose, contain two or more hydroxyl (-OH) groups making them extremely
    • soluble in water. Structural isomers: glucose and fructose have the same
    • molecular formula C6H12O6 but have a different structural formula. Ring structures:
    • all monosaccharides with at least 5 carbons e.g. glucose exist predominately in
    • the cyclic forms rather than open chained forms. Most form six membered rings
    • called pyranose rings, some five membered form rings called furanose rings.
    • They act like alcohols , aldehydes and ketones, reducing agents can reduce the
    • aldehyde or ketone carbonyl groups to an alcohol.
    • Disaccharides: Carbohydrates
    • that are composed of two monosaccharide units joined together e.g. sucrose,
    • maltose, lactose. Formation of disaccharides occur when 2 disaccharides undergo
    • a condensation reaction to produce a disaccharide with the release of water.
    • Glycosidic link: the C-O-C bond that joins two monosaccharides to produce a
    • disaccharide
    • Polysaccharides: include
    • complex carbohydrates such as starch, glycogen, cellulose, agar, pectin, gum
    • Arabic, heparin and chitin. They can be hydrolysed into smaller units. Starch:
    • storage polysaccharide for plants, a polymer of glucose monomers, made up of
    • two fractions amylose and amylopectin. Amylose: soluble in water turns blue
    • with iodine. Amylopectin: insoluble in water no colour change with iodine.
    • Glycogen: reverse carbohydrate for animals found mainly in the muscle and
    • liver. Cellulose: provides structural support in plant cell walls, cellulose
    • fibres consist of bundles of parallel polysaccharide chains held together by H
    • bonding thus providing mechanical strength, insoluble in water, no colour
    • change with iodine
  3. Slide 3

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Slides sobre Sem título, criado por Sophie Hanna em 15-06-2017.
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Sophie Hanna
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