Q: Using the information below explain why CN- is a stronger Bronsted base even though in the reaction…
A: Bronsted base is the species that accept proton.
Q: The IUAPC name of this compound is?
A: The first step in assigning the IUPAC name to an organic compound is to select the longest…
Q: If there are unshared pairs of electrons on the atoms directly attached to the aromatic ring, they…
A: We know all the activators like NH2 , OH , OR etc. are Ortho - pera directors and all the…
Q: carbons with alternating double and single bonds throughout are called annulenes. A bracketed number…
A: Annulenes are monocyclic unsubstituted hydrocarbons that contain double and single bonds at the…
Q: Which of the following compounds shown below is butylberizene? to
A: The IUPAC name of the compound given is butylbenzene.
Q: notations or notations from structures, f
A: The notations from structure of tripeptides can be drawn as
Q: How many equivalent resonance structures for the cyclopentadienyl anion can be drawn ?
A: When a molecule is represented by more than one Lewis structure, then these structures are called…
Q: The structures of two tertiary bicyclic chlorides (compoun statements is correct? CI
A: Bredt's rule states that a carbon cannot be sp2 hybridized at the bridge head position which means…
Q: ring with the effect of ……………… and are ……………………… directed towards electrophiles. Groups that are…
A: If any group increases electron density on benzene is ortho para directing. If it withdraw electron…
Q: Using example discuss SN1 reactions ?
A: SN1 reaction is a nucleophilic substitution reaction. From the name itself, S stands for…
Q: Complete the reaction shown in the image below.
A: Hydration of alkene: Alkene gives hydration reactions in presence of an acid catalyst. The reaction…
Q: Write the heterolytic and homolytic equations of cleavage in the bonds of the following compounds…
A: In homolytic fusion the bonded pair electrons shared equally and forms radicals. This homolytic…
Q: How many allylic hydrogens are in the following compound
A:
Q: State the Electrostatic potential maps of pyridine and pyrrole ?
A: Electrostatic potential maps are used to illustrate the charge distribution of the molecules in a…
Q: Add the appropriate & and ô* symbols for all polar bonds in the following structures. 8. Н Н
A: The more electronegative atom has partial negative charge and the less electronegative atom has…
Q: Provide an unambiguous name for the following compound.
A: The given structure is; The structural formula of the above structure is C11H17N.
Q: Pis) Using the templates provided draw two additional uncharged resonance structures for the…
A: Resonating Structure Resonating structures are two or more Lewis structure that collectively…
Q: How many allylic hydrogens (total number - not type!) are present in the following molecule?
A: When a compound contains atleast one double bond between two Carbon atoms, then the carbons attached…
Q: molecules and provide short descriptio: 1. H-Ņ-CH3
A: The functional group in the above compound is amine (-NH2 group). The nitrogen in the amino group is…
Q: How many additional resonance forms can be drawn for phenanthrene shown below?
A: Resonance structure is basically rearrangement of electron from one bond to adjacent bond but not…
Q: How many non-equivalent carbons exist in the following compound? (Give a number
A: Different types of spectroscopy can be used to identify the structure of unknown compound. Some…
Q: Rank the structures shown from most to least stable.
A: The given structure can be ranked from most stable to least stable
Q: Provide the name of the structure ( according to r, s if there's)
A: The name of the structure can be predicted as
Q: Label the most electrophillic carbon atom ?
A: The given compound is neral. Draw the 2d structure of this compound.
Q: Question - Highlight isoprene units in each of the molecules below:
A:
Q: Provide the best IUPAC name for the following molecules in the images below
A: Given that, We have to give the IUPAC names of the following molecules.
Q: Benzene Colto, ) was found to be totally unroactive toward addition Reactions. Based upon Resonance…
A: Here we have to explain why addition reaction of benzene is completely unreactive according to…
Q: ゲ-o
A:
Q: fill in the blanks. If there are unshared pairs of electrons on the atoms directly attached to the…
A: Explanation- 1) Electron donating groups cause the second subtituent to add on to the para or ortho…
Q: Predict the predicted product of the reaction shown in the following diagram:
A: -NH2 group is strong ring aactivation group, hence when amino benzene (aniline) is treated with…
Q: How many lone pairs are involved in sustaining the conjugation of pyridine?
A: Lone pair are not involved in conjugation in pyridine
Q: Which of the following is anti aromatic?
A: The anti aromatic compound has to be identified.
Q: of the atoms in the following diagram (attached) of allylcyanide have been randomly labelled with…
A: Steric number = 2-> linear =3 ->trigonal planar…
Q: Given the following compounds. Answer the following questions. Be sure to attach IR tables used as…
A: Infrared spectroscopy gives the fundamental structural details of the organic compound. The…
Q: What are reactants will form the enamine shown? For the following molecules classify them as…
A:
Q: Using the nomenclature guide, provide an appropriate name for the following molecule. Me Me
A:
Q: which of the following structures, if flat, would be assified as antiaromatic
A: Aromatic compounds are those that obey Huckel rule and has 4n+2 pie electrons.
Q: EN ?
A: A heterocyclic compound is a derivative of carbon-containing compounds which contain atoms other…
Q: Write an additional resonance contributing structure for each carbocation and state which of the two…
A: The generation of polarity in a molecule because of interaction of the lone pair and pi-bond that…
Q: Due to the extra unpair electron in atomic oxygen orbital, it is very much reactive than unsaturated…
A:
Q: Draw the orbital interaction that illustrates the hyperconjugation that takes place in propyne.
A: The hyper conjugation is the delocalization of the δ electron from the Cα-H bond to an adjacent…
Q: [0]
A: Given reactant is ketone and reagent is oxygen . So, reaction is oxidation reaction.
Q: Select the TWO most electrophilic carbons in this molecule. CI :
A:
Q: Which would you think would be a strongerinteraction and why: an interaction between a sodium ion…
A: Given information: an interaction between a sodium ion and the partial negative charge on the oxygen…
Q: Give the letter for the side group that would interact with cations the best.
A: Given,
Q: Using the nomenclature guide, provide an appropriate name for the following molecule. Ме Me. ОН
A: Note: According to our guidelines we are supposed to answer only one question. Kindly repost other…
Q: Write with additional resonance contributing structure for each carbocation and state which of the…
A:
Q: This question refers to the following reaction: i) Determine whether the main reaction to…
A: Substitution or elimination depends on nucleophile if which OH- is from H2O then there will be…
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Solved in 2 steps with 2 images
- Are the following pairs of structures resonance contributors or different compounds?Some of the figures below represent invalid sets of resonance structures for this molecule.Which of the following choices depicts the correct resonance arrows to show the conversion between the Q resonance form to the R resonance form?
- How many possible resonance structures can you have in total for the nitrite ion.#1: What is the formal charge of bromine in the structure of bromate, BrO3-? a) 0 b) +1 c) +2 d) -1 #2: Carbonate (CO32-) has three resonance structures. Choose the stayement that best expains the meaning of those 3 resonance structures. a) Carbonate consists of two single CO bonds and one double CO bond. b) Carbonate consists of one single structure which is an average of the three resonance structures. c) Carbonate quickly flips back and forth between three structures. d) Three different structures for carbonate coexist. #3: When compaing a carbon-carbon double bond (C==C) and a carbon-carbon single bond (C-C), the double bond is a) longer and shorter b) longer and weaker c) shorter and stronger d) shorter and weaker1) what is the formal charge of G? a. -1 b. 0 c. +1 2) what is the formal charge of the labelled atom (refer to the blue arrow)? a. -1 b. 0 c. +1
- What is the formal charge on nitrogen in the following structure?What is the formal charge of each atom (from left to right), neglecting the hydrogens, in the following resonance structure of CH2N2? Select one: a. 0, +1, −1 b. 0, −1, +1 c. −1, −1, +1 d. −1, +1, 0 e. 0, 0, 0Write the complete computation of the formal charges of the following; a. Ethanol ( CH3CH2OH) b. Chlorate ion ( ClO3-)
- What is the calculated formal charge for carbon (C) in the CNO- ion's most stable resonance state? (6C, 7N, 8O) A. -1 B. 0 C. -3 D. +1 E. +2Resonance and Formal ChargesDraw the specified number of resonance forms for the following compounds/ions and be certain to include formal charges: NO^3- (3 resonance forms) SO4^2- (3 resonance forms)which of the following molecules can exhibit equivalent resonance structures? OH- PO43- H2O or Br2