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1. release energy thru combustion 2. chemical conversion to another fuel form 3. conversion to non-fuel material |
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a fuel's use and behavior is determined by... |
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Definition
...its chemical comnposition and molecular structure |
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the study of the origin, composition and properties, and fundamental chemical rxns of fuels |
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carbon content of common fuels |
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natural gas: 75% C petroleum: ~85% C coal: 65-95% C |
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Definition
indicate an origin from living matter |
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atmospheric CO2 is taken into plants, passes thru animals, and accumulates in dead organisms, which decay and release it back into the atmosphere |
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free energy change of photosynthesis? |
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Definition
delta G= +2720 kJ VERY endothermic equilibrium constant of 1E-47! |
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What about the organic matter that doesn't completely decay? |
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Definition
organic matter which escapes complete decay is preserved and accumulated, which we can burn as fuel (releasing that energy) |
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reverse of photosynthesis rxn |
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Definition
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Why do we have large accumulations of carbon-based fuels? |
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Definition
Because most organic rxns do not go to completion |
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to maximize accumulation of carbon-based fuels... |
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Definition
1. abundant light for photosynthesis 2. warmth for fast rxns 3. minimum exposure of organic matter to oxygen |
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oxygen can participate in decay by... |
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Definition
1. direct rxn of atmospheric O2 2. direct rxn of O2 dissolved in water 3. indirectly via aerobic bacteria |
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ideal environments for life and then prevention of decay of organic matter |
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Definition
1. freshwater lakes where a bottom layer of relatively cold anearobic water lies under a layer of warmer, aerobic water 2. marine environments where up-welling of water spreads an anearobic layer over the continental shelf |
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Definition
transport of nutrients structural components of cells enzymes |
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Definition
two or more amino acids linked to each other |
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key features of protein composition and structure |
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Definition
peptide bonds are reversible contain significant amounts of oxygen and nitrogen |
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Definition
1. number of C in the chain: pentose, hexose 2. presence of aldehyde or ketone group: aldose, ketose 3. both: aldohexose, ketopentose |
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many simple saccharides are cyclic because... |
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...they contain both an alcohol and aldehyde/ketone group, so the molecule reacts with itself and forms a ring |
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hemiacetal/hemiketal + alcohol |
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Definition
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the carbon at which the hemiacetal/hemiketal forms |
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for each hemiacetal/hemiketal, two anomers exist: |
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Definition
1. alpha: OH and CH2OH are trans 2. beta: OH and CH2OH are cis |
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Definition
the acetal linkage between monosaccharide units in a polysaccharide |
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Definition
a glycoside linkage, where the monosaccharides are glucoses |
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Definition
made of glucoses linked by beta (trans) glucoside linkage |
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Definition
made of glucoses linked by alpha (cis) glucoside linkage |
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key features of carbohydrate composition and structure |
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contain cyclic structures high oxygen content (weight basis) |
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Definition
naturally occuring compounds which yield fatty acids upon hydrolysis |
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Definition
esters of long chain alcohols with fatty acids |
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Definition
esters of long chain carboxylic acids joined by glycerol |
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key features of lipid composition and structure |
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Definition
formation is reversible relatively rich in hydrogen relatively poor in oxygen |
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Definition
a constituent of cell walls that provides extra rigidity for woody plants a "bio-polymer" made of three alcohols has abundant cyclic aromatic structures and a high proportion of oxygen |
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Term
two main types of organic matter |
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Definition
1. low-oxygen chain structures (hydrocarbons, lipids), mostly from organisms living in water 2. high-oxygen cyclic structures (carbohydrates, lignin), mostly from higher plants |
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