why does Archean Methano-revivacter smithii has no pictures explain why ?
Homework Answers
Methanobrevibacter smithii is a prokaryote belonging to the domain archaea and commonly found in human guts. The archaea is hydrogenotrophic meaning that they are able to use hydrogen as their energy source. They are also able to produce methane gas.
M.smithii are unicellular organisms and their cell morphology is coccobacillus as their cell shape is intermediate between coccus which represents spherical shapes and bacillus which represents rod shapes. Many pictures are available for study on the web under the name Methanobrevibacter smithii.
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does Archean Methano-revivacter smithii has no pictures explain why
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Isomer Selectivity. Using pictures and a
maximum of 10 words, explain why only the first isomer below is
formed. (Helpful Hint: See Helpful Hint 1 above.)
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please explain all answers
thank you
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explain the answer, why does it become a ring? when does this
happen and why?
NaOH hint: product has a satom.in a ring
Isomer Selectivity. Using pictures and a maximum of 10 words, explain why only the first isomer below is formed. (Helpful Hint: See Helpful Hint 1 above.) So Yo DME 85 °C Ms 110 °C, 18h observed not observed
Isomer Selectivity. Using pictures and a
maximum of 10 words, explain why only the first isomer below is
formed. (Helpful Hint: See Helpful Hint 1 above.)
=0 DME 85 °C 2. NH3 NA 110 °C, 18h observed not observed
5. a. Draw simple band pictures to distinguish a metallic conductor from a semi-conductor. b. Explain how and why the temperature dependence of the electrical conductivity can be used to distinguish a metallic conductor from a semiconductor. c. Pure niobium oxide (NiO) is an insulator. When it is heated in the presence of oxygen gas the resulting material becomes a semiconductor. Does the oxidation of Ni(II) to Ni(III) correspond to n-doping or p-doping? Explain using band pictures.
please explain all answers
thank you
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Explain why compound į has isolatable enantiomers, but compound ii does not: HI CH2CH3 -CH-N-CH3 Bro CH2CH2CH3 CH2CH3 CH2-N : CH2CH2CH3
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