B1.1 Carbohydrates and liqids

0.0(0)
Studied by 0 people
call kaiCall Kai
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/28

encourage image

There's no tags or description

Looks like no tags are added yet.

Last updated 1:38 PM on 6/21/26
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai

No analytics yet

Send a link to your students to track their progress

29 Terms

1
New cards

Name the number of carbons in a nucleotide that bonds the 3 components

2
New cards

list the 3 types of carbon compounds and an example for each

  1. straight: saturated fatty acid

  2. branched: glycogen

  3. cyclic: cholesterol

3
New cards

what is the function of monosaccharides

  • source of ATP in cells

  • used as building blocks to make macromolecules

4
New cards

give an example of the condensation and hydrolysis of a macromolecule

fructose + glucose —> sucrose

5
New cards

what is the difference between alpha and beta glucose? what is the effect of this?

  • alpha has hydroxyl below

  • beta has hydroxyl above

  • creates diff specificity for operations such as enzymatic catalysis

6
New cards

give word equation of maltose formation from glucose. state type of bond.

alpha glucose + alpha glucose —> maltose + water

maltose bonded in1,4 glycosidic bond

7
New cards

3 contrasts of beta VS alpha glucose

beta is kiniker shape, alpha is straight

beta is rigid, alpha is flexible

beta provides structural function, alpha provides energy storage function

8
New cards

describe the solubility of glucose

  • polar due to hydroxyl

  • O in the ring is slightly negative

  • 1,4 glycosidic bonds in glucose and hydrogen bonds in water are dissolved easily, so glucose can be transported in blood or fluid between cells

9
New cards

2 reasons of glucose stability

  1. cyclic structure

  2. intramolecular bonds are all covalent —> strong. thus intermolecular bonds are also stable

10
New cards

how does glucose yield chem. energy

  • hydrolysis of: C6H12O6 + O2 —> CO2 + H2O

11
New cards

outline why polysaccharides are energy storage compounds

  • can easily add or remove glucose compounds to mobolise and build energy stores

  • insoluble due to large molecular size

12
New cards

what polysaccharides act as energy stores in plants and animals?

plants: starch

animals: glycogen

13
New cards

state how polysaccharides make good structural compounds

  • straight chains can be grouped in bundles

  • e.g. cellulose

14
New cards

state what starch is. (function, solubility, components)

  • polysaccharides

  • energy stores

  • insoluble due to size

  • composed of amylose + amylopectin

15
New cards

describe the bonds and shape of amylse and amylopectin

amylose:

  • alpha 1,4 glycosidic bonds

  • straight

amylopectin

  • alpha 1,4 glycosidic bonds cross linekd with alpha 1,6 glycosidic bonds

  • branches

16
New cards

describe glycogen

  • polysaccharide

  • energy stores

  • insoluble due to size

  • polymer of alpha glucose

  • similar bonds and structure to amylopectin, but more branches and shorter alpha 1,4 chains

17
New cards

describe cellulose

  • polysaccharides

  • sturcural function

  • in plant cell wall

  • polymer of beta glucose

  • beta 1,4 glycosidic bonds

  • alternating orientations of glucose to give straight chain shape

  • parralel chains cross linked by hydrogen bonds

18
New cards

what is the purpose of hydrogen bonds crosslinking beta glucose chains to make cellulose?

  • hydrogen bonds are hydrophobic,

  • cellulose becomes resisten to hydrolysis —> not broken down easily

  • acts as a good structural compounds

19
New cards

what are glycoproteins components and function?

  • carbs + protein

  • functions for cell-cell recognition

    • markers on the cell plasma mem identify each other and interact accordingly

20
New cards

list 4 examples of lipids and its function

  1. fat: energy stores and thermal insulation

  2. oils: energy stores

  3. waxes: plant waterproofing

  4. steroids

    1. cholesterol: membrane structure

    2. hormones: chemical signaling

21
New cards

properties of lipids (polarity, structure, bonds, solubility

  • non polar

  • hydrophobic

  • long chains or rings of C and H

  • C-C, C-H non-polar covalent bonds

  • soluble in non polar substances

  • slightly soluble in polar substances

22
New cards

describe triglycerides and phospholipid components

triglyceride

  • fats, oils

  • glycerol and 3 faty aicds

phospholipid

  • makes cell membranes

  • glycerol, phosphate and 2 fatty acids

23
New cards

contrast saturated and unsaturated fatty acids. give one example of where each can be found.

  • saturated only has single bonds, unstaurated has double and triple bonds

  • saturated has high mp, unsaturated has low mp

  • saturated is solid at rm, unsaturated in liquid at rm

    saturated: animals fats of endotherms, maintain homeostasis

    unsaturated: plant oils

24
New cards

define mono unsaturated and poly unsaturated

mono unsaturated: one double bond

poly unsaturated: >1 double bond

25
New cards

outline how triglycerides act as good energy store

  • high energy density

  • long term storage in adipose tissue

  • insoluble in H2O —> only purposefully transported

26
New cards

outline how triglycerides act for thermal regulations

  • distributed around the body for insulation

  • has low thermal conductivity

27
New cards

draw a phospholipid

  • components

  • hydrophobic/ hydrophillic

  • polarity

  • saturation

28
New cards

describe the structure and polarity of a steroid.

  • 4 ring structure

  • non polar, can pass thru phospholipid bilayer

29
New cards

describe 2 functions of a steroid

structure: cholesterol provides rigidity to cell mem

hormones: estradioland testosterone are chemical signals (hormones)