
Interpretation:
The electronic configuration and orbital diagram for bromine atom having
Concept introduction:
The number of electrons in an element is equal to its atomic number.
The orbital diagram represents the electrons in the form of an arrow. The arrows are drawn in the box and the box represents the orbital.
General rules for writing electronic configuration:
Electrons will reside in the available orbitals of lowest possible energy.
Each orbital can accommodate a maximum of two electrons.
Electrons will not pair in degenerate orbitals if an empty orbital is available.
Orbitals will fill in order of increasing energy
The electrons are filled in the increasing order of energy. The lowest energy orbitals are filled first.
In an orbital, only two electrons are present. The spin of the electrons must be opposite.
The s orbital can hold up to two electrons and the p orbital can hold up to six electrons, d-orbital can have 0–10 electrons, and f-orbital can have 0–14 electrons.
Electrons are filled according to the Hund’s rule, which states that while filling the orbitals of equal energy, first the electrons are singly filled and then, they are filled with the parallel spin.

Want to see the full answer?
Check out a sample textbook solution
Chapter 6 Solutions
Chemistry
- Predict the major products of this organic reaction.arrow_forward2. Provide the structure of the major organic product in the following reaction. Pay particular attention to the regio- and stereochemistry of your product. H3CO + H CN Aarrow_forwardPredict the major products of the following organic reaction.arrow_forward
- 1) The isoamyl acetate report requires eight paragraphs - four for comparison of isoamyl alcohol and isoamyl acetate (one paragraph each devoted to MS, HNMR, CNMR and IR) and four for comparison of acetic acid and isoamyl acetate ((one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of…arrow_forwardWhat steps might you take to produce the following product from the given starting material? CI Br Он до NH2 NH2arrow_forward1) The isoamyl acetate report requires eight paragraphs - four for comparison of isoamyl alcohol and isoamyl acetate (one paragraph each devoted to MS, HNMR, CNMR and IR) and four for comparison of acetic acid and isoamyl acetate ((one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of…arrow_forward
- №3 Fill in the below boxes. HN 1. LAH 2. H3O+ NH2arrow_forwardFor the photochemical halogenation reaction below, draw both propagation steps and include the mechanism arrows for each step. H CH ot CH3 CI-CI MM hv of CH H-CI CH3 2nd attempt See Periodic Table See Hint Draw only radical electrons; do not add lone pair electrons. Note that arrows cannot meet in "space," and must end at either bonds or at atoms. 1 i Add the missing curved arrow notation to this propagation step. 20 H ن S F P H CI Br 品arrow_forwardThe radical below can be stabilized by resonance. 4th attempt Draw the resulting resonance structure. DOCEarrow_forward
- Use curved arrows to generate a second resonance form for the allylic radical formed from 2-methyl-2-pentene. 1 Draw the curved arrows that would generate a second resonance form for this radical. D 2 H S F A Бг Iarrow_forwardDraw the resulting product(s) from the coupling of the given radicals. Inlcude all applicable electrons and non-zero formal charges. H.C öö- CH3 2nd attempt +1 : 招 H₂C CH CH₂ See Periodic Table See H H C S F P Br CH₂ Iarrow_forwardPlease, help me out with the calculation, step by step on how to find what's blank with the given information.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





