please complete an acid hydrolysis of this amide. The NH2 group connected the R group off...
please help me in all sections asap!!
Predict the product of the following reaction sequence. NaCN 1. LiAIHA HCN 2. H2O H2N NH2 но NH2 но но CN H2N H2N IV We were unable to transcribe this imagePredict the product for the following reaction. ОН excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 CH H_NHNH2 NH OH 0 CH CH NNH OH HO NHNH 0 NH IV v Predict the product of the following reaction sequence. NaCN HCN NH2 H2N но...
Draw the condensed or line-angle structural formulas for the
products from the acid- or base-catalyzed hydrolysis of each of the
following compounds.
Ht, heat CH-CH2--0-CH-CH2-CH2-CH3 + H202 H + NaOH Heat CH3 -CH2-C-0-CH3 + H2O H+, heat 2 (,–c.1=&_o 0 + 110 minit CH3 -CH2- + H2O Ht, heat 2 We were unable to transcribe this image
please help in all sections asap!!
Predict the product of the following reaction. CH3COOH ОН ОН Compound A on ozonolysis yields the following two products What is the structure of compound A? Compound A 1.03 2. (CH3)25 OV none of these Predict the product(s) for the following reaction. H30 OH We were unable to transcribe this imageA compound with an OH and an OR group attached to the same carbon is known as an acetal a hemiacetal a hydrate a...
out of the list of options what is the functional group of this
molecular structure.
i've come up with that the below is isobutane? but everything i
read shows this as an alkane and im confused why the functional
group wont match my list of options?
please can someone break this down for me.
aldehyde alkyl halide amide carboxylic acid saturated hydrocarbon unsaturated hydrocarbon We were unable to transcribe this image
. The covalent (ester / amide /hydrocarbon /hydrogen) bond between peptides is responsible for the (primary /secondary /tertiary /quaternary) structure of a protein. (Delete incorrect answers) (2 pts) 2. (a) Of the twenty amino acids, onlyof them are termed essential amino acids. (1pt (b) What does it mean when an amino acid is termed "essential"? (2 pts) 3. Draw an example of hydrogen bonding between the carbonyl group and the secondary NH group of two different amino acids in the...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
please complete each section of the
problem:a,b,c,d
#52 A simple ohmmeter is made by connecting a 1.50V flash- light battery in series with a resistance R and an ammeter that We were unable to transcribe this image
please help in all sections asap!!!!
Which of the following reagent(s) could not be used to carry out the following transformation? HSCH2CH2SH, BFy; then Raney NI (H) 1. NH NH/H"; 2. KOH/H20/heat LAH, ether Zn(Hg), HCI Predict the product for the following reaction. О, Н excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 HO. Η ΝΗΝΗΣ NH2 CH OH CH CH HOCHNHNH OH NH2 NNH2 IN V We were unable to transcribe this imagePredict the product(s) for the following reaction. NaOH...
Hi
i need to known unknown molecule, functional group, 1hnmr ,
13cnmr information and please give me information about ir spectra
using NMR data given.
Carhonyl carbons Aldehydes/Ketones Carboxylic acid derivatives (Acids, amides, esters) Pi-system carbons Aromatics Alkynes Alkenes Carbons with electronegative atoms or groups Ethers/Alcohols (X=0) lodides (X = 1) Other Groups (CI, Br, N. C=C, CHO) Alkyl carbons Methine Methylene Methyl 225 200 175 150 125 100 Chemical Shift (ppm) 75 25 Protons adjacent to electron withdrawing groups...
Could u please help me with numbers 1, 8, 9, 2, 3, 4 and also
the one under 4 numbered 1. thanks in advance
1. Which of the Fischer projections correctly depicts the following compound? To do this problem, first determine R/ configuration of the compound in question, then do same for a, b, c, d. There could be an easier way. нон ң он CHCH но н @ CH (6) CH (©) CH (@ CH нон нонн ньоннон но...