Identify the two compounds. Give an example compound, for each one, where they are found in...
Tugue compound 2. Identify the following compounds as owing compounds as a(n) alkane, alkene, alkyne, cycloalkane, or cycloalkene: _Molecule Family Molecule Family Η Η Η Η Η H-C-C-C-C-C-H CH3-CH 2 HHHH H-C-H CH3 CH3 HẠC CH3 CH-CH HC CH CH3-CH2-CH=C—CH CH3-CH-CH-CH CH₂ CH₂ CH3-CH=C=CH CH2-CH
Give the IUPAC name of each of the following compounds
aromate D) amine E) ketone 2. Give the IUPAC name of each of the following compounds: H OH HC (a) Hoc (b) CHE (c) Hoc HO (d) CH3 CHE HC (e) Ho-o (1) na CH₂ H CH₂ HyC N. CH3 HC N ( g ) сн.
1. How many different sets of "chemically equivalent
protons" are on each of these different compounds?
2. Give the splitting pattern for the designated
protons on the following molecules.
3 Which type of spectroscopy can most easily be used
to tell these two compounds apart? (Note superscripted number
denotes mass number of isotope of oxygen)
10. Identify which compound best matches the following
spectral data.
1. How many different sets of "chemically equivalent protons" are on each of these different...
Biochem: please label the following biochemical pathways with
the name of each compound, the enzyme involved in each reaction,
the byproducts of each reaction if there are any (ATP, ADP, NADH,
NADPH, FADH2, CO2, H2O etc.) and
if possible where reaction is capable of occuring (cytosol,
mitochondria, etc.) and the type of reaction (clevage,
transamination, isomerization, hydration, decarboxylation,
etc.)
Thank you
FADH, NAD FAD COA NADH, H COA COA H 1 2 3 H 4 18 NH P-ribose COA çoo...
Biochem: please label the following biochemical pathways with
the name of each compound, the enzyme involved in each reaction,
the byproducts of each reaction if there are any (ATP, ADP, NADH,
NADPH, FADH2, CO2, H2O etc.)
FADH, NAD FAD COA NADH, H COA COA H 1 2 3 H 4 18 NH P-ribose COA çoo HNICH COA CH, Coo HC 11 10 +H2O 5 coon CH COO- HC "OOC OH сн. CH 14 coo COO NADH + H 6 9...
Give the relationship of the
two compounds: Different Compounds, Same compound, Constitutional
(structural) isomers, Enantiomers, or Diastereomers
d) (4 pts) CH3 CH(CH3)2 H-CH2CH3 BrH Br H+CH2CH2 CH(CH3)2 CH3 e) (4 pts)
Writing Formulas from Names: Identify each of the following compounds as ionic or molecular and then give the correct formula for each compound.
A compound has the 'H NMR spectrum shown below. Identify the compound. 11 10 9 00 7 6 UI 4 3 2 1 O None of these compounds fit the spectrum that is shown here. CN O Me H A compound has the 'H NMR spectrum shown below. Identify the compound. 3H triplet 2H triplet 2H 11 10 9 00 7 0) 5 4 3 N 1 0 None of these compounds fit the spectrum that is shown here. A...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
1. Identify all the functional groups in the following
compounds. Circle each functional group and label each group.
Thank you!
1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Hiç O CH CH CH-C-0-CHCH, -0-CH, CH CH(CH), a. acid group СОН) -CH-CHNHA 0-C-CH Amphetamine (a central nervous system stimulant and abused drug) O Aspirin ( 13 H1802 . . HC=CHCHACHACHCH CHO CHE e. HCCHI (CH OH CHE Citronellal alcohol group ~...