1) | ||||
Date | Account Titles and Explanation | Debit | Credit | |
01-Jan-21 | Equipment (price determined below) | $ 84,813.45 | ||
Discount on notes payable (difference) | $ 15,186.55 | |||
Notes payable (face amount) | $ 1,00,000.00 | |||
Interest | $100000 x 7% x PVOA(4, 12%) = $7000 x 3.03735 | $ 21,261.45 | ||
Principal | $100000 x PV(4,12%) = 100000 x .63552 | $ 63,552.00 | ||
Present value (price) of the note | $ 84,813.45 | |||
2) | ||||
Period | Cash Payment | Effective Interest Prior Balance x 12% | Increase in Balance | Outstanding Balance |
01-Jan | $ 84,813.45 | |||
31-Dec-21 | 7000 | $ 10,177.61 | $ 3,177.61 | $ 87,991.06 |
31-Dec-22 | 7000 | $ 10,558.93 | $ 3,558.93 | $ 91,549.99 |
31-Dec-23 | 7000 | $ 10,986.00 | $ 3,986.00 | $ 95,535.99 |
31-Dec-24 | 7000 | $ 11,464.01 | $ 4,464.01 | $1,00,000.00 |
Total | 28000 | $ 43,186.55 | $ 15,186.55 | |
3) | ||||
Date | Account Titles and Explanation | Debit | Credit | |
31-Dec-23 | Interest expense | $ 10,986.00 | ||
Discount on notes payable (difference) | $ 3,986.00 | |||
Cash | $ 7,000.00 | |||
4) | Installment Payment = present value of notes /PVOA(4,12%) | |||
Installment Payment = $84,813.45/3.03735 | $ 27,923.50 | |||
5) | ||||
Period | Cash Payment | Effective Interest Prior Balance x 12% | Decrease in Balance | Outstanding Balance |
01-Jan | $ 84,813.45 | |||
31-Dec-21 | $ 27,923.50 | $ 10,177.61 | $ (17,745.89) | $ 67,067.56 |
31-Dec-22 | $ 27,923.50 | $ 8,048.11 | $ (19,875.40) | $ 47,192.17 |
31-Dec-23 | $ 27,923.50 | $ 5,663.06 | $ (22,260.44) | $ 24,931.72 |
31-Dec-24 | $ 27,923.50 | $ 2,991.78 | $ (24,931.73) | $ (0.00) |
Total | $ 1,11,694.01 | $ 26,880.56 | $ (84,813.45) | |
6) | ||||
Date | Account Titles and Explanation | Debit | Credit | |
31-Dec-23 | Interest expense | $ 5,663.06 | ||
Notes payable (difference) | $ 22,260.44 | |||
Cash | $ 27,923.50 | |||
Braxton Technologies, Inc., constructed a conveyor for A&G Warehousers that was completed and ready for use...
A variety of spectra for an organic compound with molecular formula C10H16O are presented below. The experimental accurate mass using (+) APCI source is 153.1280 u. The 1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following slides. Propose a structure for this unknown and answer or address the following questions or requirements: d. If there are still any questionable assignments, propose additional NMR experiments which would solve those questions and briefly explain specifically what correlations you...
Braxton Technologies, Inc., constructed a conveyor for A&G Warehousers that was completed and ready for use on January 1, 2021. A&G paid for the conveyor by issuing a $100,000, four-year note that specified 5% interest to be paid on December 31 of each year, and the note is to be repaid at the end of four years. The conveyor was custom-built for A&G, so its cash price was unknown. By comparison with similar transactions it was determined that a reasonable...
A variety of spectra for an organic compound with molecular formula C10H16O are presented below. The experimental accurate mass using (+) APCI source is 153.1280 u. The 1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following slides. Propose a structure for this unknown and answer or address the following questions or requirements: a. Using the most abundant isotopes of C, H and O, what are the errors in ppm and milli-Daltons for the experimental accurate mass?...
analyze this NMR & IR S23 CDC13 QE-300 240 UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
Fill out the tables below of the starting material and pure product by using the given NMR spectrums. Identify if the pure isomer of methyl nitrobenzoate as ortho, meta, or para. Complete the table below using your proton NMR spectrum of your starting material. Be sure to include all peaks. Note: The table is expandable. Use the structure below for the letter assignments in your table. Splitting Integration Assignment Peak (ppm) Other Notes -7.95 -7.92 0627 -787 785 7.30 751...
7. What kind of carbons correspond to these chemical shifts? 8. Based on this analysis, the unknown might contain the following substructure: UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
5. Based on this analysis, the compound might be or contain the following substructure: 6. How many different types of carbons appear to be present? What are the chemical shifts for these carbons? UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
3. Based on the integration of the peaks, what is the relative number of protons which make up each signal? 4. Identify any common splitting patterns. (ie. Isopropyl, ethyl, etc) UN (43 MIL.) 10.02s, 1H), 7.716.J-2 Hz. ) 2.0 11.5 11.0 10.5 10.0 9.5 9.0 8.5 8.0 7.5 7.0 6.5 6.0 4.0 3.5 3.0 2.5 20 15 100.5 0.0 -0.5 -1.0 -1.5 -2. 5.5 5.0 4.5 fl (ppm)
Braxton Technologies, Inc., constructed a conveyor for A&G Warehousers that was completed and ready for use on January 1, 2021. A&G paid for the conveyor by issuing a $175,000, four-year note that specified 8% interest to be paid on December 31 of each year, and the note is to be repaid at the end of four years. The conveyor was custom-built for A&G, so its cash price was unknown. By comparison with similar transactions it was determined that a reasonable...
Draw the structures of the Compounds 2.0 3.64 Unsat. Index = (2C+2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C, H, N quartet, 2H 1.0 7.02 6.84 2.43 2.45 1.08 1.04 a = 7.01 ppm, c = 3.64 ppm, b = 6.85 ppm, 0.5 doublet, 2H doublet, 2H singlet, 2H e = 1.06 ppm, 2.41 2.47 triplet, 3H 8, ppm 0.0 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 20 1.5...